Mwe Asia America Industries Sdn
MalaysiaFDA applicant, unverified
- Devices
- 1
What Mwe Asia America Industries Sdn makes
Mwe Asia America Industries Sdn manufactures patient examination gloves made of latex.
The company's products are Class I devices listed in the FDA 510(k) registry, and the company is based in the US.
Catalogue
Patient Examination Glove (Latex) Ref K892043
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mwe Asia America Industries Sdn have in the registry?
The registry currently lists 1 device for Mwe Asia America Industries Sdn. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mwe Asia America Industries Sdn's devices?
Among its 1 most recently registered device, Mwe Asia America Industries Sdn has devices listed in FDA 510(k) (1 device).
What risk classes do Mwe Asia America Industries Sdn's devices fall under?
Among its 1 most recently registered device, the classes recorded for Mwe Asia America Industries Sdn's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Mwe Asia America Industries Sdn in the registry?
The most recently registered devices listed for Mwe Asia America Industries Sdn include PATIENT EXAMINATION GLOVE (LATEX).