ClearanceBrief
510(k) K113558 ยท MDB System, Blood Culturing

BD BACTEC Plus Aerobic/F Culture Vials (plastic)

ApplicantBecton, Dickinson and Company, Sparks MD, US
DecisionSubstantially Equivalent, Mar 16, 2012
ReceivedDec 1, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K113558

DateFirm and productCodeLinked 510(k)
Oct 12, 2023Becton Dickinson & Co.
BD BACTEC Plus Aerobic/F Culture Vials, Catalog Number 442023
Open, Classified
MDBNone listed

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