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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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