ClearanceBrief
510(k) K060007 ยท FMI Needle, Hypodermic, Single Lumen

BD AUTOSHIELD PEN NEEDLE

ApplicantBecton, Dickinson & CO, Franklin Lakes NJ, US
DecisionSubstantially Equivalent, Mar 23, 2006
ReceivedJan 3, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060007

DateFirm and productCodeLinked 510(k)
May 24, 2007Becton Dickinson & Company
BD AutoShield Pen Needle (Re order Number : 329300)
Terminated
FMINone listed

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