ClearanceBrief
510(k) K800162 ยท HDW Diaphragm, Contraceptive (And Accessories)

ONCE TM

ApplicantG.D. Searle and Co., Walker MI, US
DecisionSubstantially Equivalent, Feb 11, 1980
ReceivedJan 25, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800162

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.