ClearanceBrief
510(k) K792049 ยท KMK Device, Intravascular Catheter Securement

I.V. STRIP

ApplicantE-Med Corp., Mchenry IL, US
DecisionSubstantially Equivalent, Nov 20, 1979
ReceivedOct 12, 1979
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K792049

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.