ClearanceBrief
510(k) K984392 ยท HIS Condom

ANSELL CONDOMS

ApplicantAnsell, Inc., Dothan AL, US
DecisionSubstantially Equivalent, Jul 21, 1999
ReceivedDec 8, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K984392

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.