ClearanceBrief
510(k) K761031 ยท DXE Catheter, Embolectomy

ELECATH ARTERIAL EMBOLECTOMY CATHETER

ApplicantElectro-Catheter Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Dec 13, 1976
ReceivedNov 15, 1976
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K761031

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.