FDA 510(k) Applications Submitted by MARTIN KAUFMAN

FDA 510(k) Number Submission Date Device Name Applicant
K101285 05/07/2010 CONSTELLATION VISION SYSTEM ALCON MANUFACTURING, LTD.
K970033 01/03/1997 MONARCH IOL DELIVERY SYSTEM ALCON LABORATORIES
K980292 01/26/1998 CATARACT LIQUEFRACTURE DEVICE ALCON LABORATORIES
K981103 03/26/1998 TURBOSONICS LIMITED REUSE ULTRASONIC TIP ALCON LABORATORIES
K120912 03/26/2012 INFINITI(R) VISION SYSTEM ALCON MANUFACTURING, LTD.
K110951 04/04/2011 27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA ALCON RESEARCH, LTD.
K981571 05/04/1998 MONARCH IOL DELIVERY SYSTEM ALCON LABORATORIES
K091777 06/17/2009 ALCON ULTRACHOPPER ALCON RESEARCH, LTD.
K962592 07/02/1996 OPHTHALAS 532 SOLID STATE PHOTOCOAGULATOR, OR EQUIVALENT LASER SYSTEMS ALCON LABORATORIES
K112425 08/23/2011 INFINITI VISION SYSTEM EVERGREEN II AUTOSERT IOL INJECTOR HANDPIECE ALCON MANUFACTURING, LTD.
K093210 10/13/2009 AQUALASE CAPSULE WASH TIP ALCON MANUFACTURING, LTD.
K093305 10/22/2009 ENHANCED ULTRA VIT PROBE ALCON RESEARCH, LTD.
K083191 10/29/2008 DETLOGIX ANNULOPLASTY RING, MODEL: 5100 EDWARDS LIFESCIENCES, LLC.
K955789 12/22/1995 ALCON SERIES 20000 LEGACY MACKOOL SYSTEM ALCON LABORATORIES
K965185 12/24/1996 ACRYPAK FOLDER ALCON LABORATORIES


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