FDA 510(k) Applications Submitted by MENICON U.S.A., INC.

FDA 510(k) Number Submission Date Device Name Applicant
K000133 01/18/2000 MENICON Z MENICON U.S.A., INC.
K972443 06/30/1997 MENICON SF-P AND MENICON Z RIGID GAS PERMEABLE CONTACT LENS MENICON U.S.A., INC.
K970019 01/02/1997 MENICON Z BIFOCAL DESIGN LENS/MENICON Z TRIFOCAL DESIGN LENS MENICON U.S.A., INC.


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