ClearanceBrief
510(k) K891786 ยท DWP Dilator, Vessel, Surgical

PTI INTRA-ART(R) CORONARY ARTERY PROBE (STERILE)

ApplicantPioneering Technologies, Inc., Wheat Ridge CO, US
DecisionSubstantially Equivalent, Oct 12, 1989
ReceivedMar 24, 1989
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K891786

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.