Victorch Meditek, Inc.
Country not established FDA establishment FEI 3003323921
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
Victorch Meditek's Hcg Test Card Ref K013678
510(k) 510(k)Victorch Hcg Test Strip Ref K013702
510(k) 510(k)
Company details
- FDA FEI number
- 3003323921
- Address
- 9715 Carroll Centre Rd Ste 103, San Diego, CA, 92126
Frequently asked questions
How many devices does VICTORCH MEDITEK, INC. have in the registry?
The registry currently lists 2 devices for VICTORCH MEDITEK, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list VICTORCH MEDITEK, INC.'s devices?
Among its 2 most recently registered devices, VICTORCH MEDITEK, INC. has devices listed in FDA 510(k) (2 devices).
What risk classes do VICTORCH MEDITEK, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for VICTORCH MEDITEK, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from VICTORCH MEDITEK, INC. in the registry?
The most recently registered devices listed for VICTORCH MEDITEK, INC. include VICTORCH MEDITEK'S HCG TEST CARD and VICTORCH HCG TEST STRIP.