ClearanceBrief
510(k) K781863 ยท HHW Pessary, Vaginal

DEVICE, FEMALE INCONTINENCE

ApplicantEschmann Bros. & Walsh , Ltd., Walker MI, US
DecisionUnknown, Nov 6, 1978
ReceivedNov 6, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781863

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.