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FDA 510(k)

DEVILBISS PULMO-AIDE COMPACT COMPRESSOR

K-Number: K020932 · 2002-06-28

ApplicantSunrise Medical
Decision Date2002-06-28
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DEVILBISS PULMO-AIDE COMPACT COMPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Sunrise Medical. It received FDA 510(k) clearance on 2002-06-28 under 510(k) number K020932. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVILBISS PULMO-AIDE COMPACT COMPRESSOR?

DEVILBISS PULMO-AIDE COMPACT COMPRESSOR is a medical device that received FDA 510(k) clearance on 2002-06-28. The listed applicant is Sunrise Medical. The 510(k) number is K020932.

When did DEVILBISS PULMO-AIDE COMPACT COMPRESSOR receive FDA 510(k) clearance?

DEVILBISS PULMO-AIDE COMPACT COMPRESSOR received FDA 510(k) clearance on 2002-06-28, under 510(k) number K020932.

Who is the listed applicant for DEVILBISS PULMO-AIDE COMPACT COMPRESSOR?

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

What is the FDA product code for DEVILBISS PULMO-AIDE COMPACT COMPRESSOR?

The FDA product code for DEVILBISS PULMO-AIDE COMPACT COMPRESSOR is CAF.

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Other records listing Sunrise Medical 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.

K123975QUICKIE & ZIPPIE SERIESK093070DEVILBISS INTELLIPAP/ SLEEPCUBE BILEVEL ST, DV56 ST SERIESK091919DEVILBISS INTELLIPAP/SLEEPCUBE BILEVEL S/STK082209DEVILBISS DV5M SMARTLINK SYSTEMK081468DEVILBISS PORTABLE OXYGEN CONCENTRATOR, 306 SERIESK071397DEVILBISS 5 LITER COMPACT OXYGEN CONCENTRATOR, MODEL 525 SERIES

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Related Devices (Code: CAF)

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.

K254171Mesh Nebulizer (UN204); Mesh Nebulizer (UN205); Mesh Nebulizer (UN209); Mesh Nebulizer (UN210)Shenzhen Mericonn Technology Co., Ltd.K260270FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)FindAir Sp. z o.o.K251572eRapid with eTrack SystemPari Respiratory Equipment, Inc.K251659Mesh Nebulizer (H6)Qingdao Future Medical Technology Co., Ltd.K244035Portable mesh nebulizer (JM821)Shenzhen Jermei Medical Device Technology Co., Ltd.K243468Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer (NB-1102); Compressor Nebulizer (NB-1103)Joytech Healthcare 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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