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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