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FDA 510(k)

BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER

K-Number: K020974 · 2002-06-26

Decision Date2002-06-26
Product CodeCBF
Advisory CommitteeAN
DecisionUnknown

Device Summary

BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER is the device name listed in this FDA 510(k) record. The listed applicant is Environmental Tectonics Corp.. It received FDA 510(k) clearance on 2002-06-26 under 510(k) number K020974. The device is classified under product code CBF. It was reviewed by the AN advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER?

BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER is a medical device that received FDA 510(k) clearance on 2002-06-26. The listed applicant is Environmental Tectonics Corp.. The 510(k) number is K020974.

When did BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER receive FDA 510(k) clearance?

BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER received FDA 510(k) clearance on 2002-06-26, under 510(k) number K020974.

Who is the listed applicant for BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER?

The FDA 510(k) record lists Environmental Tectonics Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER?

The FDA product code for BARA-MED ACRYLIC MONOPLACE HYPERBARIC 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.

Other records listing Environmental Tectonics Corp. as applicant

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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