Medical Device Manufacturer · SE , Jarfalla

Perimed AB - FDA 510(k) Cleared Devices

4 submissions · 4 cleared · Since 2001

Recent clearances: PeriFlux6000, PERIFLUX 6000, PERICAM PSI

4
Total
4
Cleared
0
Denied

FDA 510(k) Regulatory Record - Perimed AB Anesthesiology ✕

1 devices
1-1 of 1
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