3M Diagnostic Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 4
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
3M Anti-Cardiolipin Fast(Tm) Test Ref K913054
Regimes: 510(k) Registry: 510(k)3M Anti-Dsdna Fast Test Ref K913653
Regimes: 510(k) Registry: 510(k)Fasttech System 1 Ref K911496
Regimes: 510(k) Registry: 510(k)Fasttech System Ii Ref K913892
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does 3M Diagnostic Systems, Inc. have in the registry?
The registry currently lists 4 devices for 3M Diagnostic Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list 3M Diagnostic Systems, Inc.'s devices?
Among its 4 most recently registered devices, 3M Diagnostic Systems, Inc. has devices listed in FDA 510(k) (4 devices).
What risk classes do 3M Diagnostic Systems, Inc.'s devices fall under?
Among its 4 most recently registered devices, the classes recorded for 3M Diagnostic Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from 3M Diagnostic Systems, Inc. in the registry?
The most recently registered devices listed for 3M Diagnostic Systems, Inc. include 3M ANTI-CARDIOLIPIN FAST(TM) TEST, 3M ANTI-DSDNA FAST TEST, FASTTECH SYSTEM 1 and FASTTECH SYSTEM II.