ClearanceBrief
510(k) K810124 ยท DYG Catheter, Flow Directed

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ApplicantAmerican Edwards Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Feb 4, 1981
ReceivedJan 19, 1981
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K810124

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.