ClearanceBrief
510(k) K860805 ยท DQO Catheter, Intravascular, Diagnostic

PRESSURE MONITOR CATH MODELS SP5325,SP5327,SP5337

ApplicantGould, Inc., Oxnard CA, US
DecisionSubstantially Equivalent, May 8, 1986
ReceivedMar 4, 1986
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K860805

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.