MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES
K-Number: K091541 · 2009-12-31
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Device Summary
Frequently Asked Questions
What is the MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES?
MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES is a medical device that received FDA 510(k) clearance on 2009-12-31. The listed applicant is Sequal Technologies Co., Ltd.. The 510(k) number is K091541.
When did MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES receive FDA 510(k) clearance?
MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES received FDA 510(k) clearance on 2009-12-31, under 510(k) number K091541.
Who is the listed applicant for MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES?
The FDA 510(k) record lists Sequal Technologies Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES?
The FDA product code for MESA OXYGEN CONCENTRATOR, MODEL 2-6000 SERIES 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 Co., Ltd. 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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