Mnlase, Inc. - FDA 510(k) Cleared Devices
Recent clearances: MODEL 230-SAS LASER DELIVERY PROBE, CURVED ENDOPHOTOCOAGULATOR LASER PROBE, STRAIGHT ENDOPHOTOCOAGULATOR LASER PROBE
22
Total
22
Cleared
0
Denied
FDA 510(k) Regulatory Record - Mnlase, Inc. Chemistry ✕
4 devices