510(k) Report

FDA applicant

Amron International Diving Supply, Inc.

Escondido, CA1 decision2002–20020 recalls

FDA records 1 decision for Amron International Diving Supply, Inc. (Escondido, CA) in 2002: 1 510(k) clearance. All are in product code CBF (Chamber, Hyperbaric). Its devices cite 1 predicate, 0 of them its own earlier devices. 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 Amron International Diving Supply, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Amron International Diving Supply, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • CBFChamber, Hyperbaric1decision

Whose devices does it build on?

Its devices cite 1 predicate; 0 are its own earlier devices. The firms it cites most:

What has FDA decided for it lately?

  • K011592Oxygen Treatment HoodAmron International Diving Supply, Inc. · 2002

The one decision as Amron International Diving Supply, Inc. →