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FDA 510(k)

THE MILLER NEBULIZER SYSTEM

K-Number: K926055 · 1993-02-03

ApplicantWarren C. Miller
Decision Date1993-02-03
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

THE MILLER NEBULIZER SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Warren C. Miller. It received FDA 510(k) clearance on 1993-02-03 under 510(k) number K926055. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE MILLER NEBULIZER SYSTEM?

THE MILLER NEBULIZER SYSTEM is a medical device that received FDA 510(k) clearance on 1993-02-03. The listed applicant is Warren C. Miller. The 510(k) number is K926055.

When did THE MILLER NEBULIZER SYSTEM receive FDA 510(k) clearance?

THE MILLER NEBULIZER SYSTEM received FDA 510(k) clearance on 1993-02-03, under 510(k) number K926055.

Who is the listed applicant for THE MILLER NEBULIZER SYSTEM?

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

What is the FDA product code for THE MILLER NEBULIZER SYSTEM?

The FDA product code for THE MILLER NEBULIZER SYSTEM is CAF.

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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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