Sppik Rubber Industries Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Glove (Latex) Ref K891127
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Sppik Rubber Industries Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Sppik Rubber Industries Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Sppik Rubber Industries Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Sppik Rubber Industries Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Sppik Rubber Industries Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Sppik Rubber Industries Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Sppik Rubber Industries Sdn. Bhd. in the registry?
The most recently registered devices listed for Sppik Rubber Industries Sdn. Bhd. include PATIENT EXAMINATION GLOVE (LATEX).