Ameritekusa, Inc.
United Statesfrom the FDA registration address FDA establishment FEI 1000126037
- Devices
- 2
- Registrations
- FDA
- FDA recalls
- 0
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Dbest Hcg Panel Test Kit Ref K061257
Regimes: 510(k) Registry: 510(k)Dbest One Step Occult Blood Test Kits Ref K071242
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 1000126037
- Address
- 125 130th St SE Ste 200, EVERETT, WA, 98208
Frequently asked questions
How many devices does AMERITEKUSA, INC. have in the registry?
The registry currently lists 2 devices for AMERITEKUSA, INC.. Devices recorded under merged duplicate company entries are counted once.
Which registries list AMERITEKUSA, INC.'s devices?
Among its 2 most recently registered devices, AMERITEKUSA, INC. has devices listed in FDA 510(k) (2 devices).
What risk classes do AMERITEKUSA, INC.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for AMERITEKUSA, INC.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from AMERITEKUSA, INC. in the registry?
The most recently registered devices listed for AMERITEKUSA, INC. include DBEST HCG PANEL TEST KIT and DBEST ONE STEP OCCULT BLOOD TEST KITS.