VIGORMIST COMPRESSOR NEBULIZER
K-Number: K031413 · 2003-10-07
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Device Summary
Frequently Asked Questions
What is the VIGORMIST COMPRESSOR NEBULIZER?
VIGORMIST COMPRESSOR NEBULIZER is a medical device that received FDA 510(k) clearance on 2003-10-07. The listed applicant is Vega Technologies, Inc.. The 510(k) number is K031413.
When did VIGORMIST COMPRESSOR NEBULIZER receive FDA 510(k) clearance?
VIGORMIST COMPRESSOR NEBULIZER received FDA 510(k) clearance on 2003-10-07, under 510(k) number K031413.
Who is the listed applicant for VIGORMIST COMPRESSOR 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 VIGORMIST COMPRESSOR NEBULIZER?
The FDA product code for VIGORMIST COMPRESSOR NEBULIZER is BTI.
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: BTI)
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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