ClearanceBrief
510(k) K780349 ยท HDL Retractor, Vaginal

VAGINAL RETRACTOR

ApplicantEdward Weck, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 14, 1978
ReceivedMar 3, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K780349

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.