FDA 510(k) Applications Submitted by ALCON MANUFACTURING, LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K101774 06/24/2010 MONARCH III IOL DELIVERY SYSTEM; MONARCH III P CATRIDGE; MONARCH III HANDPIECE (H4) ALCON MANUFACTURING, LTD.
K063155 10/17/2006 MONARCH III IOL DELIVERY SYSTEM ALCON MANUFACTURING, LTD.
K101285 05/07/2010 CONSTELLATION VISION SYSTEM ALCON MANUFACTURING, LTD.
K120912 03/26/2012 INFINITI(R) VISION SYSTEM ALCON MANUFACTURING, LTD.
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.


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