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FDA 510(k) Applications Submitted by MICHAEL H 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.
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