ClearanceBrief
510(k) K944354 ยท HCG Device, Neurovascular Embolization

CONTOUR EMBOLI

ApplicantInterventional Therapeutics Corp., Fremont CA, US
DecisionSubstantially Equivalent, Dec 13, 1994
ReceivedAug 30, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K944354

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.