Bhc Biotech, Ltd.
CanadaFDA applicant, unverified
- Devices
- 1
What Bhc Biotech, Ltd. makes
Bhc Biotech, Ltd. manufactures the MAXI TEST, a diagnostic device designed for specific medical evaluations.
The MAXI TEST is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Maxi Test Ref K904016
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bhc Biotech, Ltd. have in the registry?
The registry currently lists 1 device for Bhc Biotech, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bhc Biotech, Ltd.'s devices?
Among its 1 most recently registered device, Bhc Biotech, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Bhc Biotech, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bhc Biotech, Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Bhc Biotech, Ltd. in the registry?
The most recently registered devices listed for Bhc Biotech, Ltd. include MAXI TEST.