ClearanceBrief
510(k) K820229 ยท DYG Catheter, Flow Directed

NORTON FLOW DIRECTED THERMODILUTION CATH

ApplicantNorton Performance Plastics Corp., Walker MI, US
DecisionSubstantially Equivalent, Feb 12, 1982
ReceivedJan 27, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820229

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.