Aisap
IsraelFDA applicant, unverified
- Devices
- 2
What Aisap makes
Aisap manufactures the AISAP Cardio V1.0, which is a medical device used for cardiovascular applications.
This device is classified as Class II and is listed in the FDA 510(k) registry. The company is based in the United States.
Catalogue
- Registry: GUDID
AISAP Cardio V1.0 Ref K234141
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Aisap have in the registry?
The registry currently lists 2 devices for Aisap. Devices recorded under merged duplicate company entries are counted once.
Which registries list Aisap's devices?
Among its 2 most recently registered devices, Aisap has devices listed in FDA 510(k) (1 device) and FDA GUDID (1 device). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Aisap's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Aisap's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Aisap in the registry?
The most recently registered devices listed for Aisap include AISAP Cardio V1.0 2.X.Y.Z and AISAP Cardio V1.0.