ClearanceBrief
510(k) K823937 ยท HIS Condom

SEMINAL COLLECTION DEVICE

ApplicantHealth Development Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Feb 24, 1983
ReceivedDec 29, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823937

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.