FDA applicant

Becton Dickinson Labware

Franklin Lakes, NJ3 decisions1999–19990 recalls

FDA records 3 decisions for Becton Dickinson Labware (Franklin Lakes, NJ) in 1999: 3 510(k) clearances. All are in product code MQK (Labware, Assisted Reproduction). 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, obstetrics and gynecology panel, where it files most

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

FDA decisions per year

No FDA decision for Becton Dickinson Labware since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Becton Dickinson Labware 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 Advanced Diagnostics 10 Becton, Dickinson and Company (BD) 5 Becton Dickinson Consumer Products 3 Becton Dickinson Biosciences 1 Becton, Dickinson and Company (Bard Access Systems… 1

Becton Dickinson Labware

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

Other applicant names beginning “Becton”