ClearanceBrief
510(k) K222068 ยท HIS Condom

Durex Penck III Regular

ApplicantRb Health (Us), LLC, Parsippany NJ, US
DecisionSubstantially Equivalent, Oct 12, 2022
ReceivedJul 14, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K222068

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.