ClearanceBrief
510(k) K925502 ยท KMK Device, Intravascular Catheter Securement

TRACE MODEL# 840, 841,842 & 845 ARM BOARD

ApplicantTrace Medical Equipment, Inc., Lisle IL, US
DecisionSubstantially Equivalent, Jan 12, 1993
ReceivedOct 30, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925502

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.