ClearanceBrief
510(k) K983473 ยท POV Semen Analysis Device

FERTILMARQ TEST KIT

ApplicantEmbryotech Laboratories, Inc., Wilmington MA, US
DecisionSubstantially Equivalent, Dec 17, 1998
ReceivedOct 2, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K983473

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.