FDA applicant

Beckman Analytical and Biotechnology Development

Fullerton, CA1 decision1994–19940 recalls

FDA records 1 decision for Beckman Analytical and Biotechnology Development (Fullerton, CA) in 1994: 1 510(k) clearance. All are in product code JQW (Station, Pipetting And Diluting, For Clinical…). 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 Beckman Analytical and Biotechnology Development’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Beckman Analytical and Biotechnology Development since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Beckman Analytical and Biotechnology Development by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Beckman”

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

Beckman Coulter, Inc. 286 Beckman Instruments, Inc. 281 Beckman-Diagnostic Systems Group 11 Beckman Coulter Ireland, Inc. 7 Beckman 6 Beckman Coulter Laboratory Systems (Suzhou) Co., Ltd. 2 Beckman Coulter Cellular 1 Beckman Coulter Biomedical GmbH 1

Beckman Analytical and Biotechnology Development

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Beckman”