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FDA 510(k)

4LYF OXYGEN CONCENTRATOR

K-Number: K872534 · 1987-10-13

ApplicantAirsep Corp.
Decision Date1987-10-13
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

4LYF OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Airsep Corp.. It received FDA 510(k) clearance on 1987-10-13 under 510(k) number K872534. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 18 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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