Grace River Ent., Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Grace River Ent., Inc. makes
Grace River Ent., Inc. makes a physiotherapy apparatus and patient examination gloves (latex).
The company's devices are classified as Class I and Class II and are listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
A Physiotherapy Apparatus Ref K902803
Regimes: 510(k) Registry: 510(k)Patient Examination Gloves (Latex) Ref K891277
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Grace River Ent., Inc. have in the registry?
The registry currently lists 2 devices for Grace River Ent., Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Grace River Ent., Inc.'s devices?
Among its 2 most recently registered devices, Grace River Ent., Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Grace River Ent., Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Grace River Ent., Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Grace River Ent., Inc. in the registry?
The most recently registered devices listed for Grace River Ent., Inc. include A PHYSIOTHERAPY APPARATUS and PATIENT EXAMINATION GLOVES (LATEX).