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FDA 510(k)

OXLIFE OXYGEN CONCENTRATOR

K-Number: K933081 · 1994-11-01

ApplicantOxlife, Inc.
Decision Date1994-11-01
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXLIFE OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Oxlife, Inc.. It received FDA 510(k) clearance on 1994-11-01 under 510(k) number K933081. 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 OXLIFE OXYGEN CONCENTRATOR?

OXLIFE OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1994-11-01. The listed applicant is Oxlife, Inc.. The 510(k) number is K933081.

When did OXLIFE OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

OXLIFE OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1994-11-01, under 510(k) number K933081.

Who is the listed applicant for OXLIFE OXYGEN CONCENTRATOR?

The FDA 510(k) record lists Oxlife, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OXLIFE OXYGEN CONCENTRATOR?

The FDA product code for OXLIFE 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 Oxlife, 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

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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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