First Light Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
The SensiTox B. anthracis Toxin Test Ref K232545
Regimes: 510(k) Registry: 510(k)SensiTox C. difficile Toxin Test Ref K193490
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does First Light Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for First Light Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list First Light Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, First Light Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do First Light Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for First Light Diagnostics, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from First Light Diagnostics, Inc. in the registry?
The most recently registered devices listed for First Light Diagnostics, Inc. include The SensiTox B. anthracis Toxin Test and SensiTox C. difficile Toxin Test.