ClearanceBrief
510(k) K941850 ยท KMK Device, Intravascular Catheter Securement

IMMOBILE NON-STERILE AND IMMOBILE A/C NON-STERILE

ApplicantTnt Moborg Intl. , Ltd., Buffalo NY, US
DecisionSubstantially Equivalent, Jul 14, 1994
ReceivedApr 14, 1994
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K941850

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.