Zhum Heng Development, Ltd.
Hong Kong SAR ChinaFDA 510(k) applicant, unverified
- Devices
- 1
What Zhum Heng Development, Ltd. makes
Zhum Heng Development, Ltd. manufactures latex examination gloves, designed for medical and clinical use to ensure sterility and barrier protection during patient examinations.
These products are classified as Class I medical devices under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Latex Examination Gloves Ref K893461
510(k) 510(k)
Frequently asked questions
How many devices does Zhum Heng Development, Ltd. have in the registry?
The registry currently lists 1 device for Zhum Heng Development, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Zhum Heng Development, Ltd.'s devices?
Among its 1 most recently registered device, Zhum Heng Development, Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Zhum Heng Development, Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Zhum Heng Development, Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Zhum Heng Development, Ltd. in the registry?
The most recently registered devices listed for Zhum Heng Development, Ltd. include LATEX EXAMINATION GLOVES.