ClearanceBrief
510(k) K812204 ยท KOH Instrument, Manual, General Obstetric-Gynecologic

UTERINE MANIPULATORS

ApplicantReznik Instruments, Walker MI, US
DecisionSubstantially Equivalent, Oct 13, 1981
ReceivedAug 4, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K812204

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.