ClearanceBrief
510(k) K882658 ยท DQO Catheter, Intravascular, Diagnostic

ANGIOSCOPE FOR PULMONARY ARTERY USE

ApplicantWashington Regulatory Services, Ringoes NJ, US
DecisionSubstantially Equivalent, Jan 26, 1989
ReceivedJun 29, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K882658

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.