Pacewell Sdn Bhd
MalaysiaFDA applicant, unverified
- Devices
- 1
What Pacewell Sdn Bhd makes
Pacewell Sdn Bhd makes patient examination gloves.
The company's portfolio, which includes Class I devices, is listed in the FDA 510k registry, and the company is based in the US.
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
Patient Examination Gloves Ref K943434
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Pacewell Sdn Bhd have in the registry?
The registry currently lists 1 device for Pacewell Sdn Bhd. Devices recorded under merged duplicate company entries are counted once.
Which registries list Pacewell Sdn Bhd's devices?
Among its 1 most recently registered device, Pacewell Sdn Bhd has devices listed in FDA 510(k) (1 device).
What risk classes do Pacewell Sdn Bhd's devices fall under?
Among its 1 most recently registered device, the classes recorded for Pacewell Sdn Bhd's devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Pacewell Sdn Bhd in the registry?
The most recently registered devices listed for Pacewell Sdn Bhd include PATIENT EXAMINATION GLOVES.