Vidamed, Inc.
Vidamed, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2002.
Top product codes for Vidamed, Inc.
Recent clearances by Vidamed, Inc.
- K014224 — PRECISION PLUS TUNA OFFICE SYSTEM
- K012587 — RF GENERATORS, DISPOSABLE CARTRIDGE KIT, DISPOSABLE CARTRIDGE, REUSABLE HANDLE, DISOISABLE HANDPIECE REUSABLE TELESCOPE
- K011787 — PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE
- K002583 — TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM
- K973366 — COBRA HAND PIECE
- K965199 — TUNA 5 CATHETER
- K965061 — VIDAMED MODEDL 7600 RF GENERATOR
- K963180 — VIDAMED RF GENERATOR DATA RECORDER
- K960918 — VIDAMED TUNA (TRANSURETHRAL NEEDLE ABLATION) SYSTEM
- K955035 — VIDAMED SERIES 7205 ELECTROSURGICAL GENERATOR
- K951245 — VIDAMED 50 ELECTROSURGICAL GENERATOR, VIDAMED AEC (ADJUSTABLE ELECTROSURGICAL CARTRIDGE) ACCESSORY
Data sourced from openFDA. This site is unofficial and independent of the FDA.