HYPERBARIC OXYGEN CHAMBER
K-Number: K790693 · 1979-07-30
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Device Summary
Frequently Asked Questions
What is the HYPERBARIC OXYGEN CHAMBER?
HYPERBARIC OXYGEN CHAMBER is a medical device that received FDA 510(k) clearance on 1979-07-30. The listed applicant is Hyperbaric Oxygen Therapy, Inc.. The 510(k) number is K790693.
When did HYPERBARIC OXYGEN CHAMBER receive FDA 510(k) clearance?
HYPERBARIC OXYGEN CHAMBER received FDA 510(k) clearance on 1979-07-30, under 510(k) number K790693.
Who is the listed applicant for HYPERBARIC OXYGEN CHAMBER?
The FDA 510(k) record lists Hyperbaric Oxygen Therapy, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HYPERBARIC OXYGEN CHAMBER?
The FDA product code for HYPERBARIC OXYGEN CHAMBER is CBF.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: CBF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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