ClearanceBrief
510(k) K862119 ยท DYG Catheter, Flow Directed

DESERET FLO-THRU INJECTATE TEMPERATURE SENSOR

ApplicantParke-Davis Co., Rochester MI, US
DecisionSubstantially Equivalent, Aug 29, 1986
ReceivedJun 3, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K862119

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.