Li Wah-Hong Kong, Inc.
Country not established
- Devices
- 1
What Li Wah-Hong Kong, Inc. makes
Li Wah-Hong Kong, Inc. manufactures latex examination gloves designed for medical and clinical use, intended to provide a barrier during patient examinations and procedures.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company operates from the United States.
Catalogue
Li Wah Latex Examination Gloves Ref K891323
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Li Wah-Hong Kong, Inc. have in the registry?
The registry currently lists 1 device for Li Wah-Hong Kong, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Li Wah-Hong Kong, Inc.'s devices?
Among its 1 most recently registered device, Li Wah-Hong Kong, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Li Wah-Hong Kong, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Li Wah-Hong Kong, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Li Wah-Hong Kong, Inc. in the registry?
The most recently registered devices listed for Li Wah-Hong Kong, Inc. include LI WAH LATEX EXAMINATION GLOVES.