FDA applicant

Becton Dickinson Advanced Diagnostics

Sparks, MD10 decisions1991–19940 recalls

FDA records 10 decisions for Becton Dickinson Advanced Diagnostics (Sparks, MD) from 1991 to 1994: 10 510(k) clearances. Most are in product codes JHI (Visual, Pregnancy Hcg, Prescription Use) and JJE (Analyzer, Chemistry (Photometric, Discrete)…). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, clinical chemistry panel, where it files most

How often FDA has decided Becton Dickinson Advanced Diagnostics’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Becton Dickinson Advanced Diagnostics since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Becton Dickinson Advanced Diagnostics by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Becton”

FDA records each applicant name separately; these may or may not be the same firm.

Becton, Dickinson & CO 342 Becton Dickinson Infusion Therapy Systems, Inc. 36 Becton Dickinson Microbiology Systems 33 Becton Dickinson Vascular Access, Inc. 25 Becton Dickinson Immunocytometry Systems 21 Becton Dickinson Vacutainer Systems 15 Becton Dickinson Diagnostic Instrument Systems 13 Becton, Dickinson and Company (BD) 5 Becton Dickinson Labware 3 Becton Dickinson Consumer Products 3 Becton Dickinson Biosciences 1 Becton, Dickinson and Company (Bard Access Systems… 1

Becton Dickinson Advanced Diagnostics

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Becton”