G5 Neocussor

The G5 Neocussor is a gentle, quiet, Directional-Stroking® model designed specifically for neonatal applications. The lungs of a neonate frequently cannot perform the cough mechanism due to…

Registry build 21.09.26

The G5 Neocussor is a gentle, quiet, Directional-Stroking® model designed specifically for neonatal applications. The lungs of a neonate frequently cannot perform the cough mechanism due to their premature condition. The G5 Neocussor provides a soothing, precise treatment to help loosen, and help mobilize secretion build-up in neonates. It is small enough to fit inside infant environmental chambers; is powered by a single “C” cell replaceable battery, and weighs less than five ounces. Comes with two (2) Directional-Stroking disposable applicators and one vibration applicator. Unit Advantages: Soft rubber end cushions unit in the event of a fall. Red Arrow indicates the direction of fluid movement. Comes with three different applicators.

1manufacturer
1catalogue number
1510(k) clearance

Who Else Makes It

Registered in Chongqing.

Chinese manufacturers registered for FDA product code BYI
Manufacturer City Province Registered as Device types
Chongqing Sonmol Technology Co., Ltd. Chongqing Chongqing Contract manufacturer 9

Record

Regulatory record for G5 Neocussor
Listed by General Physiotherapy, Inc., United States
FDA product code BYI
Device type Percussor, Powered-Electric
Device class Class 2
Regulation 21 CFR 868.5665
Record published 2019-06-25
Record revised 2020-04-15 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries manufacturing date, serial number
Sizes Weight 3 lb
Distribution end date 2020-04-14

Catalogue Numbers

Catalogue numbers for G5 Neocussor
Catalogue number Size Status
NC90 Weight 3 lb Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
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Showing 12 of 34. All products under Percussor, Powered-Electric

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K855129 1986-01-23

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