Hon Shan Development, Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Hon Shan Development, Ltd. makes
Hon Shan Development, Ltd. manufactures PROTEX patient examination gloves, which are designed for single-use medical examinations and procedures to maintain hygiene and reduce cross-contamination.
These products fall under FDA Class I devices and are listed via 510(k) clearance in the United States. The company operates from the US.
Catalogue
Protex (Patient Examination Gloves) Ref K892102
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Hon Shan Development, Ltd. have in the registry?
The registry currently lists 1 device for Hon Shan Development, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Hon Shan Development, Ltd.'s devices?
Among its 1 most recently registered device, Hon Shan Development, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Hon Shan Development, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Hon Shan Development, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Hon Shan Development, Ltd. in the registry?
The most recently registered devices listed for Hon Shan Development, Ltd. include PROTEX (PATIENT EXAMINATION GLOVES).