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FDA 510(k)

VIGORMIST COMPRESSOR NEBULIZER

K-Number: K031413 · 2003-10-07

Decision Date2003-10-07
Product CodeBTI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VIGORMIST COMPRESSOR NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is Vega Technologies, Inc.. It received FDA 510(k) clearance on 2003-10-07 under 510(k) number K031413. The device is classified under product code BTI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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