4LYF OXYGEN CONCENTRATOR
K-Number: K872534 · 1987-10-13
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Device Summary
Frequently Asked Questions
What is the 4LYF OXYGEN CONCENTRATOR?
4LYF OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1987-10-13. The listed applicant is Airsep Corp.. The 510(k) number is K872534.
When did 4LYF OXYGEN CONCENTRATOR receive FDA 510(k) clearance?
4LYF OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1987-10-13, under 510(k) number K872534.
Who is the listed applicant for 4LYF OXYGEN CONCENTRATOR?
The FDA 510(k) record lists Airsep Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 4LYF OXYGEN CONCENTRATOR?
The FDA product code for 4LYF 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 Airsep 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: 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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