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FDA 510(k)

LONGFEI LFY-I-5 OXYGEN CONCENTRATOR

K-Number: K033405 · 2005-10-18

ApplicantZhejiang Longfei Industrial Co., Ltd.
Decision Date2005-10-18
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LONGFEI LFY-I-5 OXYGEN CONCENTRATOR is the device name listed in this FDA 510(k) record. The listed applicant is Zhejiang Longfei Industrial Co., Ltd.. It received FDA 510(k) clearance on 2005-10-18 under 510(k) number K033405. 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 LONGFEI LFY-I-5 OXYGEN CONCENTRATOR?

LONGFEI LFY-I-5 OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 2005-10-18. The listed applicant is Zhejiang Longfei Industrial Co., Ltd.. The 510(k) number is K033405.

When did LONGFEI LFY-I-5 OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

LONGFEI LFY-I-5 OXYGEN CONCENTRATOR received FDA 510(k) clearance on 2005-10-18, under 510(k) number K033405.

Who is the listed applicant for LONGFEI LFY-I-5 OXYGEN CONCENTRATOR?

The FDA 510(k) record lists Zhejiang Longfei Industrial Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LONGFEI LFY-I-5 OXYGEN CONCENTRATOR?

The FDA product code for LONGFEI LFY-I-5 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.

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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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