Salter Aire Elite

Salter AIRE Elite Compressor with Nebulizer (1) 8900 & carry bag (1) 8258

Registry build 21.09.26
57manufacturers in China registered for this device type
31catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Zhejiang (19), Guangdong (17), Jiangsu (8). 7 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code CCQ
Manufacturer City Province Registered as Device types
Shanghai Joy Crown Industry Co., Ltd. Pu Dong New Area Shanghai Contract manufacturer 64
Hangzhou Fushan Medical Appliance Co., Ltd. Hangzhou Zhejiang Contract manufacturer 44
Ningbo Luke Medical Devices Co., Ltd. Yuyao Zhejiang Contract manufacturer 27
Foshan Hongfeng Co., Ltd. Foshan Guangdong Contract manufacturer 24
Polymed (Xiamen) Plastic Industrial Co., Ltd. Xiamen Fujian Contract manufacturer 17
Zhejiang Baite Medical Appliances Co., Ltd. Huzhou Zhejiang Contract manufacturer 13
Hangzhou Jinlin Medical Appliances Co., Ltd. Hangzhou Zhejiang Contract manufacturer 11
Boen Healthcare Co., Ltd. Suzhou Jiangsu Specification developer 263
Jiangsu NEW Pentastar Medical Products Co., Ltd. Changzhou Jiangsu Exporter 146
Huzhou Junda Industry Co., Ltd. Anji Zhejiang Contract manufacturer 129
Zhejiang Mediunion Healthcare Group Co., Ltd. Ningbo Zhejiang Contract manufacturer 105
Zhejiang Lidesen Medical Instrument Co., Ltd. Hangzhou Zhejiang Contract manufacturer 100

Showing 12 of 57. All 57 manufacturers in China registered for Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

Record

Regulatory record for Salter Aire Elite
Listed by Salter Labs, United States
FDA product code CCQ
Device type Nebulizer, Medicinal, Non-Ventilatory (Atomizer)
Device class Class 1
Regulation 21 CFR 868.5640
Establishment Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
510(k) K870027
Record published 2016-09-24
Record revised 2025-09-24 (version 7)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Supplied as a kit Yes
Latex Labelled latex-free
Label carries lot or batch number, serial number
Storage Storage environment temperature -15 to 50 °C; Handling environment temperature 10 to 40 °C
Distribution end date 2018-07-26

Catalogue Numbers

Catalogue numbers for Salter Aire Elite
Catalogue number Size Status
SO-1774BE In distribution
SO-1872GN In distribution
SO-1033RD In distribution
SO-1721BE In distribution
SO-1062BK In distribution
8350-8906 In distribution
SO-1931GN In distribution
SO-1049GN In distribution
SO-1005GN In distribution
SO-1867RD In distribution
8501-0-5 In distribution
SO-1441BE In distribution
8350-8900 In distribution
8353-8924-7-1 In distribution
SO-1935BK In distribution
8352-8924-7-1 In distribution
SO-1425BE In distribution
SO-1611BE In distribution
SO-1428BK In distribution
SO-1411RD In distribution
8501-1-2 In distribution
SO-1434BY In distribution
SO-1769BK In distribution
SO-1677BE In distribution
SO-1777RD In distribution
8352-8900-7-1 In distribution
8350B-8900 In distribution
SO-1773BE In distribution
SO-1755BE In distribution
SO-1647BK In distribution
SO-1011GN Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Nebulizer, Medicinal, Non-Ventilatory (Atomizer) Salter Labs 67
LMA Atomization Teleflex Medical LLC 30
silverfox Silverfox Corporation Limited 14
MedSource Nebulizer Medsource International, LLC 11
Curaplex Bound Tree Medical, LLC 7
VixOne™ Nebulizer Kit Canadian Hospital Specialties Ltd. 6
Hudson RCI Teleflex Medical LLC 6
BR Surgical, LLC BR Surgical LLC 5
1A Chamber Patejim S.R.L. 5
Fofo Foshan Hongfeng Co., Ltd. 5
Mediox Mediox Medical Service Ltd 5
Jedmed Jedmed Instrument Company 4

Showing 12 of 45. All products under Nebulizer, Medicinal, Non-Ventilatory (Atomizer)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K870027 1987-03-16
K870755 1987-03-16

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Salter Aire Elite
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
SunMed Group Holdings, LLC 510(k) number 2011-03-25 Not classified Equipment maintenance A small number of oxygen mask components were found to have 100% obstructed airways rendering them incapable of delivering oxygen to patients undergoing respiration therapy. 9000 all varieties 2011-10-26

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer