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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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