ClearanceBrief
510(k) K820759 ยท KMK Device, Intravascular Catheter Securement

VEIN-SHIELD

ApplicantPan-Tech Research, Inc., Walker MI, US
DecisionSubstantially Equivalent, May 14, 1982
ReceivedMar 22, 1982
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K820759

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.