Master & Frank Enterprise Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Master-Frank N95 Particulate Respirator Ref K172963
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Master & Frank Enterprise Co., Ltd. have in the registry?
The registry currently lists 1 device for Master & Frank Enterprise Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Master & Frank Enterprise Co., Ltd.'s devices?
Among its 1 most recently registered device, Master & Frank Enterprise Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Master & Frank Enterprise Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Master & Frank Enterprise Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Master & Frank Enterprise Co., Ltd. in the registry?
The most recently registered devices listed for Master & Frank Enterprise Co., Ltd. include Master-Frank N95 Particulate Respirator.