Home › Device types › CBF
Chamber, Hyperbaric
FDA product code CBF · Class 2 · Anesthesiology
150
Registered devices
154
Adverse events
3
Recalls
69
510(k) clearances
Devices with this code
Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.HMS-2000 — Hyperbaric Modular Systems Inc.HMS-5000-6-MINI-QUADRO — Hyperbaric Modular Systems Inc.HMS-5000 — Hyperbaric Modular Systems Inc.Summit to Sea — SUMMIT TO SEA, LLCVitaeris 320 — HYPERBARIC TECHNOLOGIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.TEKNA Manufacturing Pvt. Ltd. — TEKNA MANUFACTURING PRIVATE LIMITEDSechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Perry Baromedical — PERRY BAROMEDICAL CORPORATIONNewtowne Hyperbarics — TYPHOON WATER WARES LTDSechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Revitalair — OXAVITA S.R.L.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Hyperbaric for Life — Hyperbaric For Life.com, LlcNewtowne Hyperbarics — TYPHOON WATER WARES LTDSechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.Sechrist Industries, Inc. — SECHRIST INDUSTRIES, INC.
Recent recalls
| Date | Firm | Reason |
|---|---|---|
| 2014-08-08 | Baro-Therapies, Inc | The firm is distributing the Rejuvenator device without an approved 510(k). |
| 2008-08-28 | Sechrist Industries Inc | Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with Electronic Control Modules in order to correct a software bug that could potentiall |
| 2008-08-28 | Sechrist Industries Inc | Sechrist 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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