Fisma, Inc. - FDA 510(k) Cleared Devices
Recent clearances: DENTAL 200, DENTAL 300, DENTAL 400, MODELS E-20, E-60, E-50, ATLAS-ELITE,MODEL E-80,CORIUM 200,CORIUM 400, MODEL E-90, ELITE, MODEL E-80-II, ELITE ULTRA, MODEL E-80-IV
4
Total
4
Cleared
0
Denied
FDA 510(k) Regulatory Record - Fisma, Inc. General & Plastic Surgery ✕
4 devices
Cleared
Aug 24, 2000
VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9
General & Plastic Surgery
218d
Cleared
Jul 20, 1999
DENTAL 200, DENTAL 300, DENTAL 400, MODELS E-20, E-60, E-50
General & Plastic Surgery
84d
Cleared
Apr 01, 1999
ATLAS-ELITE,MODEL E-80,CORIUM 200,CORIUM 400, MODEL E-90, ELITE, MODEL...
General & Plastic Surgery
72d
Cleared
Nov 08, 1996
PC LASER WITH SMART PLUG (PC EDO & DENTAL 200)
General & Plastic Surgery
88d