ClearanceBrief
510(k) K052408 ยท FMI Needle, Hypodermic, Single Lumen

EZ-IO

ApplicantVidacare Corporation, Irvine CA, US
DecisionSubstantially Equivalent, Nov 17, 2005
ReceivedSep 1, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K052408

DateFirm and productCodeLinked 510(k)
Sep 22, 2014Vidacare Corporation
EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
Terminated
FMINone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.