Perimed, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PERIFLUX SYSTEM 5000 MODULAR LASER DOPPLER SYSTEM MAIN UNIT MODEL PF 5001, INCLUDING PF 5010 LDPM UNIT
6
Total
6
Cleared
0
Denied
FDA 510(k) Regulatory Record - Perimed, Inc. Cardiovascular ✕
4 devices
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
PERIFLUX PF3
Cardiovascular
119d