Vidamed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vidamed, Inc. - FDA 510(k) Cleared Devices
11
Total
11
Cleared
0
Denied
Vidamed, Inc. has 11 FDA 510(k) cleared medical devices. Based in Menlo Park, US.
Historical record: 11 cleared submissions from 1995 to 2002. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Vidamed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Vidamed, Inc.
11 devices
Cleared
Jan 23, 2002
PRECISION PLUS TUNA OFFICE SYSTEM
General & Plastic Surgery
28d
Cleared
Dec 11, 2001
RF GENERATORS, DISPOSABLE CARTRIDGE KIT, DISPOSABLE CARTRIDGE, REUSABLE...
Gastroenterology & Urology
123d
Cleared
Jul 06, 2001
PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE
Gastroenterology & Urology
28d
Cleared
Feb 13, 2001
TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM
Gastroenterology & Urology
179d
Cleared
Nov 26, 1997
COBRA HAND PIECE
Gastroenterology & Urology
79d
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