Dio-Med Corp. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
FDA 510(k) Regulatory Record - Dio-Med Corp. General & Plastic Surgery ✕
6 devices
Cleared
Mar 01, 1994
DIOMED 25 25W SURGICAL DIODE LASER
General & Plastic Surgery
223d
Cleared
Oct 19, 1993
DIOMED 25 25W SURGICAL DIODE LASER
General & Plastic Surgery
193d
Cleared
Sep 23, 1993
DIOMED 25 25W SURGICAL DIODE LASER
General & Plastic Surgery
197d
Cleared
Sep 16, 1993
DIOMED 25 SURGICAL DIODE LASER, GYNECOLOGY APPLIC
General & Plastic Surgery
707d
Cleared
Jan 22, 1993
DIOMED 25 SURGICAL DIODE LASER, UROLOGY APPLICAT
General & Plastic Surgery
470d
Cleared
Jan 15, 1993
DIOMED 25 SURGICAL DIODE LASER, GEN SURG APPLICAT
General & Plastic Surgery
463d