FDA 510(k) Applications Submitted by JOSEPH RESS

FDA 510(k) Number	Submission Date	Device Name	Applicant
K970562	02/13/1997	TENOSNARE	LUXTEC CORP.
K970642	02/20/1997	TENOSCOPE	LUXTEC CORP.
K961209	03/28/1996	BRIO AUTOMATIC SAMPLINC UNIT	SEAC S.R.L.
K991560	05/04/1999	NASO-LARYNGO-PHARYNGOSCOPE	FIBER IMAGING TECHNOLOGIES, INC.
K992040	06/17/1999	FLEXISCOPE II ARTHROSCOPES AND ACCESSORIES	FIBER IMAGING TECHNOLOGIES, INC.
K992362	07/15/1999	FLEXISCOPE IQ 101	SCHOELLY FIBEROPTIC, GMBH
K992437	07/22/1999	SCHOELLY RIGID ENDOSCOPES	FIBER IMAGING TECHNOLOGIES, INC.
K992527	07/28/1999	URETERO-RENOSCOPE	FIBER IMAGING TECHNOLOGIES, INC.
K982819	08/11/1998	ENDIUS SPINE ENDOSCOPE	ENDIUS, INC.
K973193	08/25/1997	LUXSCOPE	LUXTEC CORP.
K993300	10/01/1999	COLDLIGHTSOURCE PL3000	FIBER IMAGING TECHNOLOGIES, INC.
K984641	12/31/1998	FLEXISCOPE OPTOMODUL	SCHOELLY FIBEROPTIC, GMBH
K972873	08/04/1997	IMMUSTRIP HAMA IGG	IMMUNOMEDICS, INC.