North Atlantic Rehabilitation, Inc.
Country not established
- Devices
- 1
What North Atlantic Rehabilitation, Inc. makes
North Atlantic Rehabilitation, Inc. makes the ACTIC 2002, a device used in rehabilitation settings.
The ACTIC 2002 is a Class I medical device listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
Actic 2002 Ref K946169
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does North Atlantic Rehabilitation, Inc. have in the registry?
The registry currently lists 1 device for North Atlantic Rehabilitation, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list North Atlantic Rehabilitation, Inc.'s devices?
Among its 1 most recently registered device, North Atlantic Rehabilitation, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do North Atlantic Rehabilitation, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for North Atlantic Rehabilitation, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from North Atlantic Rehabilitation, Inc. in the registry?
The most recently registered devices listed for North Atlantic Rehabilitation, Inc. include ACTIC 2002.