Shijiazhuang Aok 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 Shijiazhuang Aok Plastic Co., Ltd. have in the registry?
The registry currently lists 1 device for Shijiazhuang Aok Plastic Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Shijiazhuang Aok Plastic Co., Ltd.'s devices?
Among its 1 most recently registered device, Shijiazhuang Aok Plastic Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Shijiazhuang Aok Plastic Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Shijiazhuang Aok Plastic Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Shijiazhuang Aok Plastic Co., Ltd. in the registry?
The most recently registered devices listed for Shijiazhuang Aok Plastic Co., Ltd. include AOK POWDER-FREE VINYL PATIENT EXAMINATION GLOVES, CLEAR (NON-COLORED).