Equatorial Rubber Mfg. Industry Sdn Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
Catalogue
Patient Examination Glove Ref K891956
510(k) 510(k)
Frequently asked questions
How many devices does Equatorial Rubber Mfg. Industry Sdn Bhd have in the registry?
The registry currently lists 1 device for Equatorial Rubber Mfg. Industry Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Equatorial Rubber Mfg. Industry Sdn Bhd's devices?
Among its 1 most recently registered device, Equatorial Rubber Mfg. Industry Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Equatorial Rubber Mfg. Industry Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Equatorial Rubber Mfg. Industry Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Equatorial Rubber Mfg. Industry Sdn Bhd in the registry?
The most recently registered devices listed for Equatorial Rubber Mfg. Industry Sdn Bhd include PATIENT EXAMINATION GLOVE.