A&J 5L POCA SERIES OXYGEN CONCENTRATOR
K-Number: K121531 · 2012-07-17
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Device Summary
Frequently Asked Questions
What is the A&J 5L POCA SERIES OXYGEN CONCENTRATOR?
A&J 5L POCA SERIES OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 2012-07-17. The listed applicant is Zhongshan A&J Medical Equipment Co., Ltd.. The 510(k) number is K121531.
When did A&J 5L POCA SERIES OXYGEN CONCENTRATOR receive FDA 510(k) clearance?
A&J 5L POCA SERIES OXYGEN CONCENTRATOR received FDA 510(k) clearance on 2012-07-17, under 510(k) number K121531.
Who is the listed applicant for A&J 5L POCA SERIES OXYGEN CONCENTRATOR?
The FDA 510(k) record lists Zhongshan A&J Medical Equipment Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for A&J 5L POCA SERIES OXYGEN CONCENTRATOR?
The FDA product code for A&J 5L POCA SERIES OXYGEN CONCENTRATOR 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 Zhongshan A&J Medical Equipment 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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