ClearanceBrief
510(k) K895530 ยท HIS Condom

STANDARD CONDOM

ApplicantMayer Laboratories, Oakland CA, US
DecisionSubstantially Equivalent, Nov 28, 1989
ReceivedSep 13, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K895530

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.