ClearanceBrief
510(k) K141256 ยท HIS Condom

OKAMOTO STUDDED CONDOM

ApplicantOkamoto USA, Inc., Washington DC, US
DecisionSubstantially Equivalent, Jul 23, 2014
ReceivedMay 14, 2014
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K141256

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.