FDA 510(k) Applications Submitted by EMBRYOTECH LABORATORIES, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K011679 05/30/2001 FERTILMARQ HOME DIAGNOSTIC SCREENING TEST KIT FOR MALE INFERTILITY EMBRYOTECH LABORATORIES, INC.
K983473 10/02/1998 FERTILMARQ TEST KIT EMBRYOTECH LABORATORIES, INC.


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