Bemiss Jason Corp.
Country not established
- Devices
- 1
What Bemiss Jason Corp. makes
Bemiss Jason Corp. makes cysto aprons in various sizes.
These devices are Class I medical devices listed in the FDA 510(k) registry, and the company is based in the United States.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Cysto Aprons In Various Sizes Ref K893842
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Bemiss Jason Corp. have in the registry?
The registry currently lists 1 device for Bemiss Jason Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Bemiss Jason Corp.'s devices?
Among its 1 most recently registered device, Bemiss Jason Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Bemiss Jason Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Bemiss Jason Corp.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Bemiss Jason Corp. in the registry?
The most recently registered devices listed for Bemiss Jason Corp. include CYSTO APRONS IN VARIOUS SIZES.