FDA applicant

Gulf States Airgas

Theodore, AL2 decisions1992–19920 recalls

FDA records 2 decisions for Gulf States Airgas (Theodore, AL) in 1992: 2 510(k) clearances. All are in product code BXK (Gas, Calibration (Specified Concentration)). 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 Gulf States Airgas’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Gulf States Airgas since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Gulf States Airgas by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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

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Other applicant names beginning “Gulf”

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

Gulf Coast Hyperbarics, Inc. 3 Gulf Medical Fiberoptics 2 Gulf South Research Institute 1 Gulf Coast Medical, Inc. 1 Gulf Medical Technologies, Inc. 1

Gulf States Airgas

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Gulf”