Vidamed, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
FDA 510(k) Regulatory Record - Vidamed, Inc. General & Plastic Surgery ✕
7 devices
Cleared
Jan 23, 2002
PRECISION PLUS TUNA OFFICE SYSTEM
General & Plastic Surgery
28d
Cleared
Apr 30, 1997
TUNA 5 CATHETER
General & Plastic Surgery
125d
Cleared
Jan 28, 1997
VIDAMED MODEDL 7600 RF GENERATOR
General & Plastic Surgery
41d
Cleared
Oct 10, 1996
VIDAMED RF GENERATOR DATA RECORDER
General & Plastic Surgery
57d
Cleared
Oct 08, 1996
VIDAMED TUNA (TRANSURETHRAL NEEDLE ABLATION) SYSTEM
General & Plastic Surgery
216d
Cleared
Nov 29, 1995
VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR
General & Plastic Surgery
27d
Cleared
Jun 09, 1995
VIDAMED 50 ELECTROSURGICAL GENERATOR, VIDAMED AEC (ADJUSTABLE ELECTROSURGICAL...
General & Plastic Surgery
84d