First Medical, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Modification To Alpha Dx System Ref K014024
Regimes: 510(k) Registry: 510(k)Alpha Dx System Ref K010562
Regimes: 510(k) Registry: 510(k)Modification To Alpha Dx System Ref K013118
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does First Medical, Inc. have in the registry?
The registry currently lists 4 devices for First Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list First Medical, Inc.'s devices?
Among its 4 most recently registered devices, First Medical, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do First Medical, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for First Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from First Medical, Inc. in the registry?
The most recently registered devices listed for First Medical, Inc. include ALPHA DX ANALYZER 01-0100, ALPHA DX MYO/CK/CK-MB/TNI CARDIAC PANEL TEST KIT 03-0001, ALPHA DX CK/CK-MB PANEL TEST KIT, MODIFICATION TO ALPHA DX SYSTEM and ALPHA DX SYSTEM.