Tung Kuang Rubber Factory Co., Ltd.
TaiwanFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves (Latex) Ref K892099
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Tung Kuang Rubber Factory Co., Ltd. have in the registry?
The registry currently lists 1 device for Tung Kuang Rubber Factory Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Tung Kuang Rubber Factory Co., Ltd.'s devices?
Among its 1 most recently registered device, Tung Kuang Rubber Factory Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Tung Kuang Rubber Factory Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Tung Kuang Rubber Factory Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Tung Kuang Rubber Factory Co., Ltd. in the registry?
The most recently registered devices listed for Tung Kuang Rubber Factory Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).