ClearanceBrief
510(k) K841705 ยท DYG Catheter, Flow Directed

WEDGE PRESSURE CATHETER FLOW DIRECTED

ApplicantMansfield Scientific, Inc., Walker MI, US
DecisionSubstantially Equivalent, Jul 13, 1984
ReceivedApr 23, 1984
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K841705

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.