ClearanceBrief
510(k) K011480 ยท HIS Condom

VIVA

ApplicantRichter Rubber Technology Sdn. Bhd., Louisville KY, US
DecisionSubstantially Equivalent, May 24, 2001
ReceivedMay 14, 2001
TypeAbbreviated
FDA recordOpen on fda.gov

Recalls that name K011480

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.