ClearanceBrief
510(k) K781558 ยท DQO Catheter, Intravascular, Diagnostic

PRESSURE MONITORING INJECTION LINES

ApplicantCobe Laboratories, Inc., Mchenry IL, US
DecisionSubstantially Equivalent, Oct 10, 1978
ReceivedSep 11, 1978
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K781558

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.