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FDA 510(k)

2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY

K-Number: K890842 · 1989-06-07

ApplicantMaico Hearing Instruments, Inc.
Decision Date1989-06-07
Product CodeEWO
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY is the device name listed in this FDA 510(k) record. The listed applicant is Maico Hearing Instruments, Inc.. It received FDA 510(k) clearance on 1989-06-07 under 510(k) number K890842. 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 2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY?

2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY is a medical device that received FDA 510(k) clearance on 1989-06-07. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K890842.

When did 2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY receive FDA 510(k) clearance?

2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY received FDA 510(k) clearance on 1989-06-07, under 510(k) number K890842.

Who is the listed applicant for 2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY?

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

What is the FDA product code for 2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY?

The FDA product code for 2400 AUDIOMETER, IMPEDANCE METER & HRNG. AID ANALY is EWO.

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Other records listing Maico Hearing Instruments, 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.

K960031AUDIOFLEX 120K954054MAICO PRODIGY CIC SERIESK953161MAICO MA630D AUDIOMETER WITH OPTIONAL REFLEX DECAY & EUSTACHIAN TUBE FUNCTIONK950637MAICO IN-THE-EAR MODEL RD-312 CICK946253MAICO IN-THE-EAR MODEL RD 201K931322KS 5 - CLINICAL AUDIOMETER

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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

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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