510(k) Report

FDA applicant

Ata Hyperbaric Chamber Manufacturing

Victoria, Bc, CA1 decision2005–20050 recalls

FDA records 1 decision for Ata Hyperbaric Chamber Manufacturing (Victoria, Bc, CA) in 2005: 1 510(k) clearance. All are in product code CBF (Chamber, Hyperbaric). 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 Ata Hyperbaric Chamber Manufacturing’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ata Hyperbaric Chamber Manufacturing since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Ata Hyperbaric Chamber Manufacturing 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

What has FDA decided for it lately?

  • K040145Ata HCM Monoplace Hyperbaric SystemAta Hyperbaric Chamber Manufacturing · 2005

The one decision as Ata Hyperbaric Chamber Manufacturing →