Ka Hung Development, Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Ka Hung Development, Ltd. makes
Ka Hung Development, Ltd. manufactures non-sterile patient examination gloves, designed for single-use medical procedures requiring barrier protection.
These gloves are classified as Class I devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Patient Examination Gloves (Non Sterile) Ref K895657
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Ka Hung Development, Ltd. have in the registry?
The registry currently lists 1 device for Ka Hung Development, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Ka Hung Development, Ltd.'s devices?
Among its 1 most recently registered device, Ka Hung Development, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Ka Hung Development, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Ka Hung Development, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Ka Hung Development, Ltd. in the registry?
The most recently registered devices listed for Ka Hung Development, Ltd. include PATIENT EXAMINATION GLOVES (NON STERILE).