ClearanceBrief
510(k) K851078 ยท DYB Introducer, Catheter

HDC SILCATH SUBCLAVIAN CATHETER PERCUTANEOUS INSER

ApplicantHdc Corp., Mountain View CA, US
DecisionSubstantially Equivalent, Apr 19, 1985
ReceivedMar 18, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K851078

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.