Brytech, Inc.
CanadaFDA 510(k) applicant, unverified
- Devices
- 1
What Brytech, Inc. makes
Brytech, Inc. manufactures the SENSORY 6, which is a medical device.
The company is based in the United States, and its product is classified as Class I and listed in the FDA 510(k) registry.
Catalogue
Sensory 6 Ref K862338
510(k) 510(k)
Frequently asked questions
How many devices does Brytech, Inc. have in the registry?
The registry currently lists 1 device for Brytech, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Brytech, Inc.'s devices?
Among its 1 most recently registered device, Brytech, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Brytech, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Brytech, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Brytech, Inc. in the registry?
The most recently registered devices listed for Brytech, Inc. include SENSORY 6.