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FDA 510(k)

LIF-O-GEN #3000 OXYGEN CONCENTRATOR

K-Number: K812693 · 1981-10-13

ApplicantLif-O-Gen, Inc.
Decision Date1981-10-13
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LIF-O-GEN #3000 OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Lif-O-Gen, Inc.. It received FDA 510(k) clearance on 1981-10-13 under 510(k) number K812693. 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 LIF-O-GEN #3000 OXYGEN CONCENTRATOR?

LIF-O-GEN #3000 OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1981-10-13. The listed applicant is Lif-O-Gen, Inc.. The 510(k) number is K812693.

When did LIF-O-GEN #3000 OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

LIF-O-GEN #3000 OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1981-10-13, under 510(k) number K812693.

Who is the listed applicant for LIF-O-GEN #3000 OXYGEN CONCENTRATOR?

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

What is the FDA product code for LIF-O-GEN #3000 OXYGEN CONCENTRATOR?

The FDA product code for LIF-O-GEN #3000 OXYGEN CONCENTRATOR is CAW.

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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.

K254289Portable Oxygen Concentrator (OX-1A-E, OX-1B)Oxytek Medical Technology Co., Ltd.K260171Portable Oxygen Concentrator (PO1 5B, PO1 6B)BMC Medical Co., Ltd.K252399Portable Oxygen ConcentratorHonsun (Nantong) Co., Ltd.K252965Oxygen Concentrator (OX-5A, OX-5C)Oxytek Medical Technology Co., Ltd.K252407OxyGo Portable Oxygen Concentrator (1400-7000)Mv Life, LLCK253549DeVilbiss 5 Liter Oxygen Concentrator (555)Devilbiss Healthcare, LLC

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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