Biohytech International, Inc.
United StatesFDA applicant, unverified
- Devices
- 7
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Rnp Eia Diagnostic Kit Ref K870457
Regimes: 510(k) Registry: 510(k)Ss-Dna Eia Diagnostic Kit Ref K870452
Regimes: 510(k) Registry: 510(k)Histones Eia Diagnostic Kit Ref K870458
Regimes: 510(k) Registry: 510(k)Dnp Eia Diagnostic Kit Ref K870456
Regimes: 510(k) Registry: 510(k)Ds-Dna Eia Diagnostic Kit Ref K870453
Regimes: 510(k) Registry: 510(k)Ana-Enzyme Immunoassay (Ana-Eia) Diagnostic Kit Ref K862969
Regimes: 510(k) Registry: 510(k)Sm Eia Diagnostic Kit Ref K870455
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Biohytech International, Inc. have in the registry?
The registry currently lists 7 devices for Biohytech International, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Biohytech International, Inc.'s devices?
Among its 7 most recently registered devices, Biohytech International, Inc. has devices listed in FDA 510(k) (7 devices).
What risk classes do Biohytech International, Inc.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Biohytech International, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Biohytech International, Inc. in the registry?
The most recently registered devices listed for Biohytech International, Inc. include RNP EIA DIAGNOSTIC KIT, SS-DNA EIA DIAGNOSTIC KIT, HISTONES EIA DIAGNOSTIC KIT and DNP EIA DIAGNOSTIC KIT.