FDA 510(k) Applications Submitted by MICHAEL SOUTHWORTH

FDA 510(k) Number	Submission Date	Device Name	Applicant
K961310	04/04/1996	STORZ PREMIERE II MICROSURGICAL SYSTEM (CX SERIES)	STORZ INSTRUMENT CO.
K960003	01/02/1996	STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION	STORZ INSTRUMENT CO.
K960024	01/02/1996	STORZ D7120 PHACO HANDPIECE MAINTENANCE KIT & STORZ D7125 PHACO HANDPIECE NEEDLE WRENCH	STORZ INSTRUMENT CO.
K080613	03/04/2008	CLEAR-VU SYSTEM, MODELS: CVL-01-1000, CVL-01-1030, CVL-01-1045	MINIMALLY INVASIVE DEVICES LLC
K954816	10/20/1995	STORZ DP4800 DELUXE , STORZ DP4801 BASIC W/REFLUX, DP4801 BASIC POSTERIOR VITRECTOMY PACK WITH VARIABLE PORT CUTTER & RX	STORZ INSTRUMENT CO.