ClearanceBrief
510(k) K072747 ยท HIS Condom

UNIDUS MAGNUM MALE LATEX CONDOM

ApplicantUnidus Corp., Tuscaloosa AL, US
DecisionSubstantially Equivalent, Nov 15, 2007
ReceivedSep 27, 2007
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K072747

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.