FDA applicant

Emox 911 CC

Somerset West, ZA2 decisions1999–19990 recalls

FDA records 2 decisions for Emox 911 CC (Somerset West, ZA) in 1999: 2 510(k) clearances. Most are in product codes MGQ (Dressing, Wound And Burn, Hydrogel W/Drug…) and CAW (Generator, Oxygen, Portable). 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 Emox 911 CC’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Emox 911 CC since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Emox 911 CC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Emox 911 CC

Which product codes does it file in?

What has FDA decided for it lately?