ClearanceBrief
510(k) K024337 ยท POV Semen Analysis Device

GENERAL SEMEN ANALYSIS (GSA) KIT

ApplicantBioshaf , Ltd., Rockville MD, US
DecisionSubstantially Equivalent, Jul 3, 2003
ReceivedDec 27, 2002
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K024337

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.