Medical Device Manufacturer · US , San Luis Obispo , CA

Biopro (M) Sdn Bhd - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1998

Total

Cleared

Denied

Biopro (M) Sdn Bhd has 5 FDA 510(k) cleared medical devices. Based in San Luis Obispo, US.

Historical record: 5 cleared submissions from 1998 to 2000. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Biopro (M) Sdn Bhd Filter by specialty or product code using the sidebar.

Biopro (M) Sdn Bhd is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Biopro (M) Sdn Bhd

5 devices

1-5 of 5