FDA applicant

Bartels & Stout, Inc.

Bellevue, WA3 decisions1981–19810 recalls

FDA records 3 decisions for Bartels & Stout, Inc. (Bellevue, WA) in 1981: 3 510(k) clearances. Most are in product codes DHN (Antinuclear Antibody, Indirect…) and GQL (Antisera, Fluorescent, Herpesvirus Hominis 1,2). 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, microbiology panel, where it files most

How often FDA has decided Bartels & Stout, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bartels & Stout, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bartels & Stout, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Bartels”

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

Bartels Immunodiagnostic Supplies, Inc. 35 Bartels, Inc. 2 Bartels Prognostics, Inc. 1

Bartels & Stout, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bartels”