FDA applicant

Marquette Gas Analysis Corp.

St. Louis, MO2 decisions1989–19910 recalls

FDA records 2 decisions for Marquette Gas Analysis Corp. (St. Louis, MO) from 1989 to 1991: 2 510(k) clearances. All are in product code CCK (Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase). 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 Marquette Gas Analysis Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Marquette Gas Analysis Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Marquette Gas Analysis Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Marquette Gas Analysis Corp.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Marquette”

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

Marquette Electronics, Inc. 82 Marquette Medical, Inc. 17 Marquette Medical Systems, Inc. 9

Marquette Gas Analysis Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Marquette”