510(k) Report

FDA applicant

Becton Dickinson Microbiology Systems

Cockeysville, MD33 decisions1992–199911 recalls

FDA records 33 decisions for Becton Dickinson Microbiology Systems (Cockeysville, MD) from 1992 to 1999: 33 510(k) clearances. Most are in product codes JTN (Susceptibility Test Discs, Antimicrobial) and JWY (Manual Antimicrobial Susceptibility Test Systems). Its devices cite 2 predicates, 0 of them its own earlier devices. 11 recalls are linked to its devices.

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

FIG. A — Illustration, microbiology panel, where it files most

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

FDA decisions per year

No FDA decision for Becton Dickinson Microbiology Systems since 2007.

Recalls per year

3in 2024

2010: 12012: 12013: 12014: 22015: 22024: 3
2007high 3 (2024) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Becton Dickinson Microbiology Systems 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.