ClearanceBrief
510(k) K900460 ยท DQO Catheter, Intravascular, Diagnostic

MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER

ApplicantNovoste Corp., Aguadilla PR, US
DecisionSubstantially Equivalent, Jul 17, 1990
ReceivedJan 30, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900460

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.