Ameritus

ACCUTEMP DISP.SKIN PROBE#210(USE ON C100,C550) w/120P probe cover

Registry build 21.09.26
3manufacturers in China registered for this device type
3catalogue numbers in this listing
2510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (2), Guangdong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code FMT
Manufacturer City Province Registered as Device types
Vincent Medical (Dong Guan) Manufacturing Co., Ltd. Dong Guan Guangdong Contract manufacturer 29
Amphenol (Changzhou) Connector Systems Co., Ltd. Changzhou Jiangsu Contract manufacturer 4
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57

Record

Regulatory record for Ameritus
Listed by Kentec Medical, LLC, United States
FDA product code FMT
Device type Warmer, Infant Radiant
Device class Class 2
Regulation 21 CFR 880.5130
Establishment Specification developer, Complaint-file establishment, Manufacturer
510(k) K960080
Record published 2016-08-02
Record revised 2018-07-06 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number
Packaging Box of 10

Catalogue Numbers

Catalogue numbers for Ameritus
Catalogue number Size Status
232 In distribution
230 In distribution
210 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
DeRoyal Deroyal Industries, Inc. 37
Fisher & Paykel Healthcare Fisher & Paykel Healthcare, Ltd. 9
AirLife™ AirLife Finland Oy 8
Tarry Probes Tarry Medical Products, Inc. 5
Argyle Cardinal Health 5
Panda Datex-Ohmeda, Inc. 4
AccuTemp Probe Kentec Medical, LLC 3
AirLife Carefusion Finland 320 Oy 3
F&P Neopuff Fisher & Paykel Healthcare, Ltd. 2
Sunflower Warmer, Stand AC120V Atom Medical Corporation 2
Heating Element 540W-104V RPI 2
Sunflower Warmer, Wall Mount AC120V Atom Medical Corporation 2

Showing 12 of 39. All products under Warmer, Infant Radiant

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K970686 1997-08-25
K960080 1996-05-01

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