Genesis Medical Interventional, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Genesis Medical Interventional F.A.S.T. (Facilitated Aspiration/Suction Thrombectomy) Systems Ref K040010
Regimes: 510(k) Registry: 510(k)F.A.S.T. System Sed And Cxd Ref K092623
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Genesis Medical Interventional, Inc. have in the registry?
The registry currently lists 2 devices for Genesis Medical Interventional, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Genesis Medical Interventional, Inc.'s devices?
Among its 2 most recently registered devices, Genesis Medical Interventional, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Genesis Medical Interventional, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Genesis Medical Interventional, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Genesis Medical Interventional, Inc. in the registry?
The most recently registered devices listed for Genesis Medical Interventional, Inc. include GENESIS MEDICAL INTERVENTIONAL F.A.S.T. (FACILITATED ASPIRATION/SUCTION THROMBECTOMY) SYSTEMS and F.A.S.T. SYSTEM SED AND CXD.