Medical Device Manufacturer · US , Wayne , NJ

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

2 submissions · 2 cleared · Since 2012
2
Total
2
Cleared
0
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
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