FDA 510(k) Applications Submitted by LENSTEC, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K091915 06/30/2009 FLUID ISOLATION DEVICE LENSTEC, INC.
K122848 09/18/2012 LENSTEC LC INJECTION SYSTEM LENSTEC, INC.
K063802 12/22/2006 LENSTEC LC INJECTION SYSTEM LENSTEC, INC.
K060533 02/28/2006 LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM LENSTEC, INC.
K050638 03/11/2005 LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSES LENSTEC, INC.


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