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FDA 510(k)

A&D UN-231 ULTRASONIC HANDY NEBULIZER

K-Number: K941627 · 1995-12-28

ApplicantA & D Corporate
Decision Date1995-12-28
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

A&D UN-231 ULTRASONIC HANDY NEBULIZER is the device name listed in this FDA 510(k) record. The listed applicant is A & D Corporate. It received FDA 510(k) clearance on 1995-12-28 under 510(k) number K941627. 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 A&D UN-231 ULTRASONIC HANDY NEBULIZER?

A&D UN-231 ULTRASONIC HANDY NEBULIZER is a medical device that received FDA 510(k) clearance on 1995-12-28. The listed applicant is A & D Corporate. The 510(k) number is K941627.

When did A&D UN-231 ULTRASONIC HANDY NEBULIZER receive FDA 510(k) clearance?

A&D UN-231 ULTRASONIC HANDY NEBULIZER received FDA 510(k) clearance on 1995-12-28, under 510(k) number K941627.

Who is the listed applicant for A&D UN-231 ULTRASONIC HANDY NEBULIZER?

The FDA 510(k) record lists A & D Corporate as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A&D UN-231 ULTRASONIC HANDY NEBULIZER?

The FDA product code for A&D UN-231 ULTRASONIC HANDY NEBULIZER 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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