ClearanceBrief
510(k) K861305 ยท HDR Cap, Cervical

INTRAUTERINE CATHETER

ApplicantRam Development, Israel, IL
DecisionSubstantially Equivalent, Dec 11, 1986
ReceivedApr 7, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K861305

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.