ClearanceBrief
510(k) K830788 ยท DQO Catheter, Intravascular, Diagnostic

CENTRAL VEIN CATHERIZATION KIT-14-690-

ApplicantNorton Performance Plastics Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Apr 30, 1983
ReceivedMar 14, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830788

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.