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FDA 510(k)

ULTRA-NEB 100 ULTRASONIC NEBULIZER

K-Number: K851695 · 1985-06-05

ApplicantThe Devilbiss Co.
Decision Date1985-06-05
Product Code
DecisionSubstantially Equivalent

Device Summary

ULTRA-NEB 100 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 1985-06-05 under 510(k) number K851695. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTRA-NEB 100 ULTRASONIC NEBULIZER?

ULTRA-NEB 100 ULTRASONIC NEBULIZER is a medical device that received FDA 510(k) clearance on 1985-06-05. The listed applicant is The Devilbiss Co.. The 510(k) number is K851695.

When did ULTRA-NEB 100 ULTRASONIC NEBULIZER receive FDA 510(k) clearance?

ULTRA-NEB 100 ULTRASONIC NEBULIZER received FDA 510(k) clearance on 1985-06-05, under 510(k) number K851695.

Who is the listed applicant for ULTRA-NEB 100 ULTRASONIC NEBULIZER?

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

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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-AIDEK872826ULTRA-NEB 99 ULTRASONIC NEBULIZERK872470DEVO/MC44 OXYGEN CONCENTRATORK854520PULMO-AIDE MODEL 5610DK852209DEVO/MC29 OXYGEN CONCENTRATOR MC29D

View all 12 devices →

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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