Gaw Rubber Products Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves (Latex) Ref K892072
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Gaw Rubber Products Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Gaw Rubber Products Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Gaw Rubber Products Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Gaw Rubber Products Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Gaw Rubber Products Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Gaw Rubber Products Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Gaw Rubber Products Sdn. Bhd. in the registry?
The most recently registered devices listed for Gaw Rubber Products Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).