INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10
K-Number: K042262 · 2004-09-10
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Device Summary
Frequently Asked Questions
What is the INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10?
INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10 is a medical device that received FDA 510(k) clearance on 2004-09-10. The listed applicant is Sequal Technologies, Inc.. The 510(k) number is K042262.
When did INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10 receive FDA 510(k) clearance?
INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10 received FDA 510(k) clearance on 2004-09-10, under 510(k) number K042262.
Who is the listed applicant for INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10?
The FDA 510(k) record lists Sequal Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10?
The FDA product code for INTEGRA OXYGEN CONCENTRATOR, MODEL 6323A-OM-10 is CAW.
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 Sequal Technologies, Inc. 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: CAW)
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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