ClearanceBrief
510(k) K891350 ยท HDC Tenaculum, Uterine

NEWPORT CERVICAL MANIPULATOR

ApplicantSimpson/Basye, Inc., Wilmington DE, US
DecisionSubstantially Equivalent, Mar 29, 1989
ReceivedMar 10, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891350

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.