Rubbertech Industry Co., Ltd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Rubbertech Industry Co., Ltd. makes
Rubbertech Industry Co., Ltd. makes latex patient examination gloves.
These devices are classified as Class I and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Latex Patient Examination Gloves Ref K895743
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Rubbertech Industry Co., Ltd. have in the registry?
The registry currently lists 1 device for Rubbertech Industry Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Rubbertech Industry Co., Ltd.'s devices?
Among its 1 most recently registered device, Rubbertech Industry Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Rubbertech Industry Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Rubbertech Industry Co., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Rubbertech Industry Co., Ltd. in the registry?
The most recently registered devices listed for Rubbertech Industry Co., Ltd. include LATEX PATIENT EXAMINATION GLOVES.