FDA applicant

Chambers & Sadler Mfg.

Mchenry, IL1 decision1978–19780 recalls

FDA records 1 decision for Chambers & Sadler Mfg. (Mchenry, IL) in 1978: 1 510(k) clearance. All are in product code BXP (Transducer, Gas Flow). 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 Chambers & Sadler Mfg.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Chambers & Sadler Mfg. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Chambers & Sadler Mfg.

Which product codes does it file in?

What has FDA decided for it lately?