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FDA 510(k)

ULTRA-NEB 99 ULTRASONIC NEBULIZER

K-Number: K872826 · 1987-09-04

ApplicantThe Devilbiss Co.
Decision Date1987-09-04
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ULTRA-NEB 99 ULTRASONIC NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is The Devilbiss Co.. It received FDA 510(k) clearance on 1987-09-04 under 510(k) number K872826. 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 ULTRA-NEB 99 ULTRASONIC NEBULIZER?

ULTRA-NEB 99 ULTRASONIC NEBULIZER is a medical device that received FDA 510(k) clearance on 1987-09-04. The listed applicant is The Devilbiss Co.. The 510(k) number is K872826.

When did ULTRA-NEB 99 ULTRASONIC NEBULIZER receive FDA 510(k) clearance?

ULTRA-NEB 99 ULTRASONIC NEBULIZER received FDA 510(k) clearance on 1987-09-04, under 510(k) number K872826.

Who is the listed applicant for ULTRA-NEB 99 ULTRASONIC NEBULIZER?

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

What is the FDA product code for ULTRA-NEB 99 ULTRASONIC NEBULIZER?

The FDA product code for ULTRA-NEB 99 ULTRASONIC NEBULIZER is CAF.

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Other records listing The Devilbiss Co. 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.

K874041DEVILBISS MODEL 8500DK872094VACU-AIDEK872470DEVO/MC44 OXYGEN CONCENTRATORK854520PULMO-AIDE MODEL 5610DK852209DEVO/MC29 OXYGEN CONCENTRATOR MC29DK851695ULTRA-NEB 100 ULTRASONIC NEBULIZER

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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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