ClearanceBrief
510(k) K830363 ยท LJF Device, Antimicrobial Drug Removal

BACTEC 170 TRYPTIC SOY BROTH W/RESINS

ApplicantBd Becton Dickinson Vacutainer Systems Preanalytic, Washington DC, US
DecisionSubstantially Equivalent, Mar 24, 1983
ReceivedFeb 4, 1983
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K830363

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.