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FDA 510(k)

AUDIOTRAVELLER, MODEL AA222

K-Number: K022728 · 2002-10-11

Decision Date2002-10-11
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

AUDIOTRAVELLER, MODEL AA222 is the device name listed in this FDA 510(k) record. The listed applicant is Interacoustics A/S, Assens. It received FDA 510(k) clearance on 2002-10-11 under 510(k) number K022728. The device is classified under product code ETY. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUDIOTRAVELLER, MODEL AA222?

AUDIOTRAVELLER, MODEL AA222 is a medical device that received FDA 510(k) clearance on 2002-10-11. The listed applicant is Interacoustics A/S, Assens. The 510(k) number is K022728.

When did AUDIOTRAVELLER, MODEL AA222 receive FDA 510(k) clearance?

AUDIOTRAVELLER, MODEL AA222 received FDA 510(k) clearance on 2002-10-11, under 510(k) number K022728.

Who is the listed applicant for AUDIOTRAVELLER, MODEL AA222?

The FDA 510(k) record lists Interacoustics A/S, Assens as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AUDIOTRAVELLER, MODEL AA222?

The FDA product code for AUDIOTRAVELLER, MODEL AA222 is ETY.

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 Interacoustics A/S, Assens 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: ETY)

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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