BARA-MED ACRYLIC MONOPLACE HYPERBARIC CHAMBER
K-Number: K020974 · 2002-06-26
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Device Summary
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
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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