Mnlase, Inc. - FDA 510(k) Cleared Devices
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mnlase, Inc. General & Plastic Surgery ✕
17 devices
Cleared
Nov 09, 1994
MODEL 230-SAS LASER DELIVERY PROBE
General & Plastic Surgery
50d
Cleared
Nov 03, 1994
CURVED ENDOPHOTOCOAGULATOR LASER PROBE
General & Plastic Surgery
55d
Cleared
Nov 03, 1994
STRAIGHT ENDOPHOTOCOAGULATOR LASER PROBE
General & Plastic Surgery
55d
Cleared
Nov 03, 1994
MODEL 210-AC ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 210-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 220-SC CURVED ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 220-SS LASER DELIVERY PROBE
General & Plastic Surgery
44d
Cleared
Nov 03, 1994
MODEL 230-SAC LASER DELIVERY PROBE
General & Plastic Surgery
44d
Cleared
Nov 01, 1994
LASER DELIVERY PROBE
General & Plastic Surgery
60d
Cleared
Nov 01, 1994
CURVD ENDOPHOTOCOGULATOR LASER PROBE
General & Plastic Surgery
53d
Cleared
Nov 01, 1994
MODEL 110-AC ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
42d
Cleared
Nov 01, 1994
MODEL 110-AS ASPIRATING ENDOPHOTOCOAGULATOR LASER
General & Plastic Surgery
42d