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FDA 510(k)

MODEL 6200 OXYGEN CONCENTRATOR

K-Number: K813320 · 1981-12-31

ApplicantHudson Oxygen Therapy Sales Co.
Decision Date1981-12-31
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODEL 6200 OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1981-12-31 under 510(k) number K813320. 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 6200 OXYGEN CONCENTRATOR?

MODEL 6200 OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1981-12-31. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K813320.

When did MODEL 6200 OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

MODEL 6200 OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1981-12-31, under 510(k) number K813320.

Who is the listed applicant for MODEL 6200 OXYGEN CONCENTRATOR?

The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL 6200 OXYGEN CONCENTRATOR?

The FDA product code for MODEL 6200 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

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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