ClearanceBrief
510(k) K981860 ยท KMK Device, Intravascular Catheter Securement

A P HARNESS

ApplicantParaworks Enterprise, Ltd., Vancouver, British Columbia, CA
DecisionSubstantially Equivalent, Jun 3, 1999
ReceivedMay 27, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K981860

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.