FDA 510(k) Applications for Medical Device Product Code: JOS (Electrode, Electrosurgical)

FDA 510(k) Applications for Medical Device Product Code "JOS"
(Electrode, Electrosurgical)

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