ClearanceBrief
510(k) K910880 ยท KMK Device, Intravascular Catheter Securement

COMFOR-BOARD

ApplicantMedway, Franklin TN, US
DecisionSubstantially Equivalent, Jun 6, 1991
ReceivedMar 1, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K910880

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.