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FDA 510(k)

MODEL 300D HOME OXYGEN LIQUEFIER

K-Number: K071461 · 2007-08-21

ApplicantCopd Partners, Inc.
Decision Date2007-08-21
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 300D HOME OXYGEN LIQUEFIER is the device name listed in this FDA 510(k) record. The listed applicant is Copd Partners, Inc.. It received FDA 510(k) clearance on 2007-08-21 under 510(k) number K071461. 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 MODEL 300D HOME OXYGEN LIQUEFIER?

MODEL 300D HOME OXYGEN LIQUEFIER is a medical device that received FDA 510(k) clearance on 2007-08-21. The listed applicant is Copd Partners, Inc.. The 510(k) number is K071461.

When did MODEL 300D HOME OXYGEN LIQUEFIER receive FDA 510(k) clearance?

MODEL 300D HOME OXYGEN LIQUEFIER received FDA 510(k) clearance on 2007-08-21, under 510(k) number K071461.

Who is the listed applicant for MODEL 300D HOME OXYGEN LIQUEFIER?

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

What is the FDA product code for MODEL 300D HOME OXYGEN LIQUEFIER?

The FDA product code for MODEL 300D HOME OXYGEN LIQUEFIER 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.

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Other records listing Copd Partners, 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.

K072011COPD LIQUID OXYGEN PORTABLE, MODEL 300P

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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