Cappel Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Antinuclear Antibody Test Ref K872839
Regimes: 510(k) Registry: 510(k)Cappel Diagnostics Ana Kit Ref K862821
Regimes: 510(k) Registry: 510(k)Anti-Ndna Antibody Test Kit Ref K864275
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cappel Diagnostics, Inc. have in the registry?
The registry currently lists 3 devices for Cappel Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cappel Diagnostics, Inc.'s devices?
Among its 3 most recently registered devices, Cappel Diagnostics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cappel Diagnostics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cappel Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cappel Diagnostics, Inc. in the registry?
The most recently registered devices listed for Cappel Diagnostics, Inc. include ANTINUCLEAR ANTIBODY TEST, CAPPEL DIAGNOSTICS ANA KIT and ANTI-NDNA ANTIBODY TEST KIT.