Medical Device Manufacturer · US , Piscataway , NJ

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

6 submissions · 6 cleared · Since 1989

6

Total

6

Cleared

0

Denied

FDA 510(k) Regulatory Record - Perimed, Inc. Cardiovascular ✕

4 devices

1-4 of 4

Cleared May 28, 1998

PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001,...

Cardiovascular · 195d

Cleared Dec 07, 1993

PERITEMP PF 4005 HEATER

Cardiovascular · 222d

Cleared Feb 03, 1993

PERIFLUX PF4001 LASER DOPPLER FLOWMETER

Cardiovascular · 259d

Cleared Jun 20, 1989

Cardiovascular · 119d