Cabin Plastic Co., Ltd.
ChinaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cabin Plastic Co., Ltd. have in the registry?
The registry currently lists 1 device for Cabin Plastic Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cabin Plastic Co., Ltd.'s devices?
Among its 1 most recently registered device, Cabin Plastic Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Cabin Plastic Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cabin Plastic Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cabin Plastic Co., Ltd. in the registry?
The most recently registered devices listed for Cabin Plastic Co., Ltd. include POWDER FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED).