Diomed, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Diomed, Inc. General & Plastic Surgery ✕
5 devices
Cleared
Dec 01, 2004
EVLT KIT AND THE D15PLUS AND D30PLUS DIODE LASERS
General & Plastic Surgery
133d
Cleared
Dec 02, 2002
EVLT KIT AND D15PLUS AND D30PLUS DIODE
General & Plastic Surgery
41d
Cleared
Nov 16, 2001
DIOMED 15 PLUS AND DIOMED 30PLUS LASERS
General & Plastic Surgery
25d
Cleared
May 01, 2000
A100 AESTHETIC DIODE LASER
General & Plastic Surgery
35d
Cleared
Feb 26, 1999
DIOSCAN
General & Plastic Surgery
53d