VEGA ULTRASONIC NEBULIZER
K-Number: K002831 · 2001-05-23
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Device Summary
Frequently Asked Questions
What is the VEGA ULTRASONIC NEBULIZER?
VEGA ULTRASONIC NEBULIZER is a medical device that received FDA 510(k) clearance on 2001-05-23. The listed applicant is Vega Technologies, Inc.. The 510(k) number is K002831.
When did VEGA ULTRASONIC NEBULIZER receive FDA 510(k) clearance?
VEGA ULTRASONIC NEBULIZER received FDA 510(k) clearance on 2001-05-23, under 510(k) number K002831.
Who is the listed applicant for VEGA ULTRASONIC NEBULIZER?
The FDA 510(k) record lists Vega Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VEGA ULTRASONIC NEBULIZER?
The FDA product code for VEGA 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 Vega Technologies, Inc. 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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