FDA 510(k) Applications Submitted by SPECIALITIES REMEEX INTERNATIONAL, S.L.

FDA 510(k) Number Submission Date Device Name Applicant
K062341 08/10/2006 MALE REMEEX SYSTEM SPECIALITIES REMEEX INTERNATIONAL, S.L.
K033310 10/14/2003 REMEEX SYSTEM FOR URINARY INCONTINENCE SPECIALITIES REMEEX INTERNATIONAL, S.L.
K063136 10/16/2006 NEEDLELESS SLING SPECIALITIES REMEEX INTERNATIONAL, S.L.


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