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FDA 510(k) Applications Submitted by MENTOR CORPORATION
FDA 510(k) Number
Submission Date
Device Name
Applicant
K050148
01/24/2005
MENTOR ARIS TRANS-OBTURATOR TAPE AND SURGICAL KIT
MENTOR CORPORATION
K052440
09/06/2005
MENTOR SELF-CATH HYDROGEL INTERMITTENT CATHETER
MENTOR CORPORATION
K053296
11/25/2005
MENTOR ARIS SUPRAPUBIC SURGICAL KIT
MENTOR CORPORATION
K062421
08/18/2006
MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER
MENTOR CORPORATION
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