FDA applicant

Swisco, Inc.

Lake Charles, LA3 decisions1988–19880 recalls

FDA records 3 decisions for Swisco, Inc. (Lake Charles, LA) in 1988: 3 510(k) clearances. Most are in product codes BYK (Tent, Oxygen, Electrically Powered) and CHL (Electrode Measurement, Blood-Gases (Pco2, Po2)…). 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 Swisco, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Swisco, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Swisco, Inc.

Which product codes does it file in?

What has FDA decided for it lately?