FDA 510(k) Number |
Applicant |
Device Name |
Decision Date |
K971187 |
AARON MEDICAL INDUSTRIES |
STANDARD & EXTENDED BLADE/NEEDLE/BALL;MODIFIED STANDARD & EXTENDED BLADE/NEEDLE |
05/05/1997 |
K974735 |
AARON MEDICAL INDUSTRIES |
STANDARD AND EXTENDED BLADE, NEEDLE AND BALL; MODIFIED STANDARD AND EXTENDED BLADE & NEEDLE; STANDARD 45 DEGREE BLADE |
06/24/1998 |
K050923 |
CONMED LINVATEC |
LIGHTWAVE INTEGRATED ELECTRODE ABLATOR AND LIGHT WAVE INTEGRATED ELECTRODE SUCTION ABLATOR |
05/18/2005 |
K962544 |
DSP WORLDWIDE |
MICRO DIAMOND-POINT DISSECTION NEEDLES |
09/20/1996 |
K003403 |
HIGHLAND / MARIETTA, INC. |
ENDOSCOPIC MONOPOLAREECTRODE, MODEL EME- 1000 TO 1999 |
05/07/2001 |
K991830 |
LINVATEC CORP. |
CAPSULAR SHRINKAGE ELECTRODE |
08/20/1999 |
K993885 |
LINVATEC CORP. |
ULTRABLATOR ELECTRODE |
02/10/2000 |
K011515 |
MEDLINE INDUSTRIES, INC. |
MEDLINE GROUNDING PAD |
07/13/2001 |
K161600 |
OLYMPUS WINTER & IBE GMBH |
Resection Electrodes |
09/06/2016 |
K962313 |
RADIOTHERAPEUTICS CORP. |
MODIFIED LEVEEN NEEDLE ELECTRODE |
09/11/1996 |
K955636 |
SENTRY MEDICAL PRODUCTS, INC. |
SENTRY DISPOSABLE DISPERSIVE ELECTRODE |
03/27/1996 |
K012684 |
STERILMED, INC. |
REPROCESSED ELECTROSURGICAL ELECTRODE |
01/18/2002 |
K000333 |
TRIAD SURGICAL TECHNOLOGIES, INC. |
STANDARD & EXTENDED BLADE, STANDARD & EXTENDED NEEDLE, STANDARD & EXTENDED BALL, MODIFIED STANDARD & EXTENDED BLADE, MOD |
05/03/2000 |
K973554 |
VALLEY FORGE SCIENTIFIC CORP. |
VALLEY FORGE BIPOLAR BALL TIP ELECTRODE |
12/19/1997 |