FDA 510(k) Applications Submitted by VIDAMED, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K960918 |
03/06/1996 |
VIDAMED TUNA (TRANSURETHRAL NEEDLE ABLATION) SYSTEM |
VIDAMED, INC. |
| K963180 |
08/14/1996 |
VIDAMED RF GENERATOR DATA RECORDER |
VIDAMED, INC. |
| K965061 |
12/18/1996 |
VIDAMED MODEDL 7600 RF GENERATOR |
VIDAMED, INC. |
| K965199 |
12/26/1996 |
TUNA 5 CATHETER |
VIDAMED, INC. |
| K973366 |
09/08/1997 |
COBRA HAND PIECE |
VIDAMED, INC. |
| K002583 |
08/18/2000 |
TUNA (TRANS URETHRA NEEDLE) OFFICE SYSTEM |
VIDAMED, INC. |
| K011787 |
06/08/2001 |
PRECISION TUNA OFFICE SYSTEM WITH NO RECTAL TEMPERATURE MONITORING TAPE |
VIDAMED, INC. |
| K012587 |
08/10/2001 |
RF GENERATORS, DISPOSABLE CARTRIDGE KIT, DISPOSABLE CARTRIDGE, REUSABLE HANDLE, DISOISABLE HANDPIECE REUSABLE TELESCOPE |
VIDAMED, INC. |
| K014224 |
12/26/2001 |
PRECISION PLUS TUNA OFFICE SYSTEM |
VIDAMED, INC. |
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