FDA applicant

Ffrench Pocket Emergency Airway, Inc.

New Orleans, LA1 decision1997–19970 recalls

FDA records 1 decision for Ffrench Pocket Emergency Airway, Inc. (New Orleans, LA) in 1997: 1 510(k) clearance. All are in product code BWC (Needle, Emergency Airway). 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 Ffrench Pocket Emergency Airway, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Ffrench Pocket Emergency Airway, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Ffrench Pocket Emergency Airway, Inc.’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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Ffrench Pocket Emergency Airway, Inc.

Which product codes does it file in?

What has FDA decided for it lately?