ClearanceBrief
510(k) K792628 ยท EFQ Gauze/Sponge, Internal

STERILIZATION PROCESS/VAGINAL SPONGE

ApplicantProcter & Gamble Mfg. Co., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 11, 1980
ReceivedDec 19, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792628

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.