ClearanceBrief
510(k) K980019 ยท HIS Condom

HTL MALE CONDOM

ApplicantReddy Medtech Health Products , Ltd., Chennai, IN
DecisionSubstantially Equivalent, Apr 1, 1998
ReceivedJan 2, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980019

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.