G.W. Healthcare, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What G.W. Healthcare, Inc. makes
G.W. Healthcare, Inc. manufactures manual and powered hospital beds, including models like the GER 540, GER 541, and the Healthcare Model #175/176 series. These beds are designed for patient positioning and mobility in clinical settings, with options for pneumatic, electric, and hydraulic operation.
The company’s products are regulated under FDA’s 510(k) pathway, with devices classified as Class I and Class II. These beds are listed in the FDA’s 510(k) database, adhering to U.S. medical device regulations.
Catalogue
Ger 540, Ger 541 Manual Bed Ref K812600
Regimes: 510(k) Registry: 510(k)Pneumatic/Electric/Hydraulic Bed Ref K831821
Regimes: 510(k) Registry: 510(k)Healthcare Model #175/176 Bed Series Ref K830559
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does G.W. Healthcare, Inc. have in the registry?
The registry currently lists 3 devices for G.W. Healthcare, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list G.W. Healthcare, Inc.'s devices?
Among its 3 most recently registered devices, G.W. Healthcare, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do G.W. Healthcare, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for G.W. Healthcare, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from G.W. Healthcare, Inc. in the registry?
The most recently registered devices listed for G.W. Healthcare, Inc. include GER 540, GER 541 MANUAL BED, PNEUMATIC/ELECTRIC/HYDRAULIC BED and HEALTHCARE MODEL #175/176 BED SERIES.