Cymun Development Sdn Bhd
MalaysiaFDA 510(k) applicant, unverified
- Devices
- 1
Catalogue
Patient Examination Glove (Latex) Ref K891881
510(k) 510(k)
Frequently asked questions
How many devices does Cymun Development Sdn Bhd have in the registry?
The registry currently lists 1 device for Cymun Development Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cymun Development Sdn Bhd's devices?
Among its 1 most recently registered device, Cymun Development Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Cymun Development Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Cymun Development Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cymun Development Sdn Bhd in the registry?
The most recently registered devices listed for Cymun Development Sdn Bhd include PATIENT EXAMINATION GLOVE (LATEX).