USE 77 ULTRASONIC NEBULIZER
K-Number: K832086 · 1983-07-19
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Device Summary
Frequently Asked Questions
What is the USE 77 ULTRASONIC NEBULIZER?
USE 77 ULTRASONIC NEBULIZER is a medical device that received FDA 510(k) clearance on 1983-07-19. The listed applicant is Medlog GmbH Marketing Services. The 510(k) number is K832086.
When did USE 77 ULTRASONIC NEBULIZER receive FDA 510(k) clearance?
USE 77 ULTRASONIC NEBULIZER received FDA 510(k) clearance on 1983-07-19, under 510(k) number K832086.
Who is the listed applicant for USE 77 ULTRASONIC NEBULIZER?
The FDA 510(k) record lists Medlog GmbH Marketing Services as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for USE 77 ULTRASONIC NEBULIZER?
The FDA product code for USE 77 ULTRASONIC NEBULIZER is CAF.
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.
Other records listing Medlog GmbH Marketing Services 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.
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.
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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