FDA 510(k) Applications Submitted by FERTILIGENT, LTD

FDA 510(k) Number Submission Date Device Name Applicant
K141666 06/23/2014 FERTILIGENT SLOW RELEASE IUI CATHETER KIT FERTILIGENT, LTD
K092579 08/17/2009 INTRAUTERINE INSEMINATION (IUI) CATHETER FERTILIGENT, LTD


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