FDA 510(k) Applications Submitted by MEDEL S.P.A.

FDA 510(k) Number Submission Date Device Name Applicant
K072494 09/05/2007 AG-CLASSIC MEDEL S.P.A.
K060404 02/15/2006 AG-PLUS, MODEL 91210 MEDEL S.P.A.
K081463 05/23/2008 MEBBY GENTLEFEED DUO BREAST PUMP/DUAL EXPRESSER PUMP MEDEL S.P.A.
K063103 10/10/2006 AG-EDGE, MODEL 91200 MEDEL S.P.A.


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