ClearanceBrief
510(k) K781819 ยท DQO Catheter, Intravascular, Diagnostic

POST EXTRA SYSTOLIC POTENTIATOR

ApplicantMedrad, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Jan 15, 1979
ReceivedOct 27, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781819

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.