Medical Device Manufacturer · SE , Jarfalla

Perimed AB - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001
4
Total
4
Cleared
0
Denied

Perimed AB has 4 FDA 510(k) cleared medical devices. Based in Jarfalla, SE.

Historical record: 4 cleared submissions from 2001 to 2016. Primary specialty: Cardiovascular.

Browse the FDA 510(k) cleared devices submitted by Perimed AB Filter by specialty or product code using the sidebar.

4 devices
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All4 Cardiovascular 3 Anesthesiology 1