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FDA 510(k)

ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER

K-Number: K962012 · 1996-08-21

ApplicantEthical Hearing Instruments
Decision Date1996-08-21
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER is the device name listed in this FDA 510(k) record. The listed applicant is Ethical Hearing Instruments. It received FDA 510(k) clearance on 1996-08-21 under 510(k) number K962012. The device is classified under product code EWO. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER?

ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER is a medical device that received FDA 510(k) clearance on 1996-08-21. The listed applicant is Ethical Hearing Instruments. The 510(k) number is K962012.

When did ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER receive FDA 510(k) clearance?

ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER received FDA 510(k) clearance on 1996-08-21, under 510(k) number K962012.

Who is the listed applicant for ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER?

The FDA 510(k) record lists Ethical Hearing Instruments as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER?

The FDA product code for ETHICAL HEARING INSTRUMENTS/WIZARD HEARING PROFILE TESTER is EWO.

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.

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Other records listing Ethical Hearing Instruments 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.

K964680COMFORTAID HEARING AID

Related Devices (Code: EWO)

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.

K234095OtoNova/OtoNova ProOtodynamicsK240430Otoport ProOtodynamics, Ltd.K231545hearOAEHearx SA (Pty) , Ltd.K213345Sentiero, AuDX, AuDX PRO, Sentiero Desktop, AuDX PRO Flex, Sentiero Advanced, NavPRO ONEPath Medical GmbHK191372LyraInteracoustics A/SK180287GSI CortiGrason-Stadler, Inc.

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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