FDA Device Intelligence
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Chamber, Hyperbaric

FDA product code CBF · Class 2 · Anesthesiology

144
Registered devices
153
Adverse events
3
Recalls
69
510(k) clearances

Devices with this code

Recent recalls

DateFirmReason
2014-08-08Baro-Therapies, IncThe firm is distributing the Rejuvenator device without an approved 510(k).
2008-08-28Sechrist Industries IncSechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentiall
2008-08-28Sechrist Industries IncSechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentiall

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