Medical Device Manufacturer · US , Piscataway , NJ

Perimed, Inc. - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 1989

Recent clearances: PERIMED TRANSCUTANEOUS PO2 AND PCO2 MONITOR (PF5040), PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT, PF404/409/410/411/416/418 W/PF319:0/319:1/319:2

View 6 510(k) Devices ↓

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Perimed, Inc. General & Plastic Surgery ✕

1 devices

1-1 of 1

Cleared Apr 18, 1994

PF404/409/410/411/416/418 W/PF319:0/319:1/319:2

General & Plastic Surgery · 154d