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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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