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FDA 510(k)

OXYGEN DIVERTER VALVE

K-Number: K033914 · 2004-04-22

ApplicantResmed, Ltd.
Decision Date2004-04-22
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OXYGEN DIVERTER VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Resmed, Ltd.. It received FDA 510(k) clearance on 2004-04-22 under 510(k) number K033914. The device is classified under product code BZD. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OXYGEN DIVERTER VALVE?

OXYGEN DIVERTER VALVE is a medical device that received FDA 510(k) clearance on 2004-04-22. The listed applicant is Resmed, Ltd.. The 510(k) number is K033914.

When did OXYGEN DIVERTER VALVE receive FDA 510(k) clearance?

OXYGEN DIVERTER VALVE received FDA 510(k) clearance on 2004-04-22, under 510(k) number K033914.

Who is the listed applicant for OXYGEN DIVERTER VALVE?

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

What is the FDA product code for OXYGEN DIVERTER VALVE?

The FDA product code for OXYGEN DIVERTER VALVE is BZD.

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Related Devices (Code: BZD)

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.

K261262Altis Full Face MaskRespironics, Inc.K253044RXiBreeze PAP System (RXiBreeze 20C)Resvent Medical Technology Co., Ltd.K253553OrionResmed CorpK254104ResScan EssentialsResmed CorpK251920Sleep Apnea Breathing Therapy Mask:JoyMask 20-B Full Face Mask, JoyMask 21-B Full Face MaskDcstar, Inc.K253166F6S Full Face Mask (F6S); P6S Nasal Pillows Interface (P6S)BMC Medical Co., Ltd.

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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