ClearanceBrief
510(k) K894415 ยท HGL Transducer, Ultrasonic, Obstetric

DYMAX ENDOVAGINAL BIOPSY GUIDE

ApplicantDymax Corp, Pittsburgh PA, US
DecisionSubstantially Equivalent, Oct 25, 1989
ReceivedJul 17, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K894415

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.