ClearanceBrief
510(k) K973780 ยท HIS Condom

PERSONAL LUBRICATING LIQUID

ApplicantQualis, Inc., Des Moines IA, US
DecisionSubstantially Equivalent, Nov 26, 1997
ReceivedOct 3, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K973780

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.