ClearanceBrief
510(k) K823758 ยท DQO Catheter, Intravascular, Diagnostic

CENTRAL VEIN CATHERIZATION KIT

ApplicantAccess Devices, Inc., Chadds Ford PA, US
DecisionSubstantially Equivalent, Feb 23, 1983
ReceivedDec 14, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K823758

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.