Medical Device Manufacturer · US , Wayne , NJ

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

2 submissions · 2 cleared · Since 2012

Total

Cleared

Denied

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

Historical record: 2 cleared submissions from 2012 to 2013. Primary specialty: General & Plastic Surgery.

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

2 devices

1–2 of 2

Data Source

FDA 510(k) public files . 174,402 total devices indexed.