Adam
FranceFDA applicant, unverified
- Devices
- 1
What Adam makes
Adam manufactures the PhysioGard SM 785, a medical device designed for patient monitoring and respiratory support, specifically targeting critical care environments.
The PhysioGard SM 785 is classified as a Class II device under FDA regulations and is listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Physiogard Sm 785 Ref K885177
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Adam have in the registry?
The registry currently lists 1 device for Adam. Devices recorded under merged duplicate company entries are counted once.
Which registries list Adam's devices?
Among its 1 most recently registered device, Adam has devices listed in FDA 510(k) (1 device).
What risk classes do Adam's devices fall under?
Among its 1 most recently registered device, the classes recorded for Adam's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Adam in the registry?
The most recently registered devices listed for Adam include PHYSIOGARD SM 785.