Grandtech Rubber Products Co., Ltd.
Hong Kong SAR ChinaFDA applicant, unverified
- Devices
- 1
What Grandtech Rubber Products Co., Ltd. makes
Grandtech Rubber Products Co., Ltd. manufactures latex patient examination gloves designed for clinical use, ensuring barrier protection during medical procedures.
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 (Latex) Ref K891972
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Grandtech Rubber Products Co., Ltd. have in the registry?
The registry currently lists 1 device for Grandtech Rubber Products Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Grandtech Rubber Products Co., Ltd.'s devices?
Among its 1 most recently registered device, Grandtech Rubber Products Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Grandtech Rubber Products Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Grandtech Rubber Products Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Grandtech Rubber Products Co., Ltd. in the registry?
The most recently registered devices listed for Grandtech Rubber Products Co., Ltd. include PATIENT EXAMINATION GLOVES (LATEX).