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Catheter, Nasal, Oxygen

FDA product code BZB · Class 1 · Anesthesiology

14
Registered devices
25
Adverse events
1
Recalls
8
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2024-11-273B Medical, Inc.The devices were inadvertently shipped after their expiration date.

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Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

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Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.