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. General & Plastic Surgery ✕
1 devices