Penfirst Corp. Sdn. Bhd.
MalaysiaFDA applicant, unverified
- Devices
- 1
What Penfirst Corp. Sdn. Bhd. makes
Penfirst Corp. Sdn. Bhd. makes patient examination gloves made of latex.
The company's devices are classified as Class I and are listed in the FDA 510(k) registry; the company is based in the United States.
Catalogue
Patient Examination Gloves (Latex) Ref K891246
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Penfirst Corp. Sdn. Bhd. have in the registry?
The registry currently lists 1 device for Penfirst Corp. Sdn. Bhd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Penfirst Corp. Sdn. Bhd.'s devices?
Among its 1 most recently registered device, Penfirst Corp. Sdn. Bhd. has devices listed in FDA 510(k) (1 device).
What risk classes do Penfirst Corp. Sdn. Bhd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Penfirst Corp. Sdn. Bhd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Penfirst Corp. Sdn. Bhd. in the registry?
The most recently registered devices listed for Penfirst Corp. Sdn. Bhd. include PATIENT EXAMINATION GLOVES (LATEX).