ClearanceBrief
510(k) K770119 ยท KMK Device, Intravascular Catheter Securement

I.V. LOK TM

ApplicantJelco Laboratories, Mchenry IL, US
DecisionSubstantially Equivalent, Mar 14, 1977
ReceivedJan 21, 1977
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K770119

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.