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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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