Cal-Tech Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Direct Acu-Slide Test Ref K861212
Regimes: 510(k) Registry: 510(k)Mono Acu-Slide Test Ref K861211
Regimes: 510(k) Registry: 510(k)Acu-Slide-Test Ref K853247
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cal-Tech Diagnostics, Inc. have in the registry?
The registry currently lists 3 devices for Cal-Tech Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cal-Tech Diagnostics, Inc.'s devices?
Among its 3 most recently registered devices, Cal-Tech Diagnostics, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Cal-Tech Diagnostics, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Cal-Tech Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cal-Tech Diagnostics, Inc. in the registry?
The most recently registered devices listed for Cal-Tech Diagnostics, Inc. include DIRECT ACU-SLIDE TEST, MONO ACU-SLIDE TEST and ACU-SLIDE-TEST.