Kev Connecticut Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Kev Connecticut Diagnostics, Inc. makes
Kev Connecticut Diagnostics, Inc. makes diagnostic devices, including VISI-NEISSERIA and VISI-STREP.
The company's portfolio is regulated as Class I devices and is listed in the FDA 510(k) registry, with the company based in the US.
Catalogue
Visi-Neisseria Ref K913456
Regimes: 510(k) Registry: 510(k)Visi-Strep Ref K910537
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Kev Connecticut Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Kev Connecticut Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Kev Connecticut Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Kev Connecticut Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Kev Connecticut Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Kev Connecticut Diagnostics, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Kev Connecticut Diagnostics, Inc. in the registry?
The most recently registered devices listed for Kev Connecticut Diagnostics, Inc. include VISI-NEISSERIA and VISI-STREP.