Medical Device Manufacturer · US , Bozeman , MT

Quantel S.A. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2008

Total

Cleared

Denied

Quantel S.A. has 2 FDA 510(k) cleared medical devices. Based in Bozeman, US.

Historical record: 2 cleared submissions from 2008 to 2010. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Quantel S.A. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Quantel S.A.

2 devices

1-2 of 2