Sharplan Lasers, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000), SHARPLAN EPITOUCH RUBY LASER SYSTEM, SHARPLAN EPITOUCH ALEXANDRITE LASER SYSTEM (5000)
78
Total
78
Cleared
0
Denied
FDA 510(k) Regulatory Record - Sharplan Lasers, Inc. Radiology ✕
1 devices