FDA applicant

Bruel & Kjaer Instruments, Inc.

Marlborough, MA4 decisions1982–19910 recalls

FDA records 4 decisions for Bruel & Kjaer Instruments, Inc. (Marlborough, MA) from 1982 to 1991: 4 510(k) clearances. Most are in product codes CBS (Analyzer, Gas, Halothane, Gaseous-Phase…) and LNN (Unnamed device). 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, anesthesiology panel, where it files most

How often FDA has decided Bruel & Kjaer Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Bruel & Kjaer Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Bruel & Kjaer Instruments, 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 “Bruel”

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

Bruel & Kjaer 4 Bruel & Kjaer Industri A/S 4

Bruel & Kjaer Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Bruel”