Zibo Boxiang Plastic & Rubber Co., Ltd.
Country not established
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Powder-Free Vinyl Patient Examination Gloves Ref K092790
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Zibo Boxiang Plastic & Rubber Co., Ltd. have in the registry?
The registry currently lists 1 device for Zibo Boxiang Plastic & Rubber Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zibo Boxiang Plastic & Rubber Co., Ltd.'s devices?
Among its 1 most recently registered device, Zibo Boxiang Plastic & Rubber Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Zibo Boxiang Plastic & Rubber Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Zibo Boxiang Plastic & Rubber Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zibo Boxiang Plastic & Rubber Co., Ltd. in the registry?
The most recently registered devices listed for Zibo Boxiang Plastic & Rubber Co., Ltd. include POWDER-FREE VINYL PATIENT EXAMINATION GLOVES.