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FDA 510(k)

AUTOSET SPIRIT CPAP SYSTEM

K-Number: K013843 · 2002-07-16

ApplicantResmed Corp
Decision Date2002-07-16
Product CodeBZD
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AUTOSET SPIRIT CPAP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Resmed Corp. It received FDA 510(k) clearance on 2002-07-16 under 510(k) number K013843. 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 AUTOSET SPIRIT CPAP SYSTEM?

AUTOSET SPIRIT CPAP SYSTEM is a medical device that received FDA 510(k) clearance on 2002-07-16. The listed applicant is Resmed Corp. The 510(k) number is K013843.

When did AUTOSET SPIRIT CPAP SYSTEM receive FDA 510(k) clearance?

AUTOSET SPIRIT CPAP SYSTEM received FDA 510(k) clearance on 2002-07-16, under 510(k) number K013843.

Who is the listed applicant for AUTOSET SPIRIT CPAP SYSTEM?

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

What is the FDA product code for AUTOSET SPIRIT CPAP SYSTEM?

The FDA product code for AUTOSET SPIRIT CPAP SYSTEM is BZD.

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 Resmed Corp 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.

K261360EasyCare Tx 2K253553OrionK254104ResScan EssentialsK251889myAirK251657Personalized Therapy Comfort Settings (PTCS)K250624myAir

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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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