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FDA 510(k)

SERIES MCAXX (MODEL 851) ITE HEARING AID

K-Number: K903583 · 1990-10-09

Decision Date1990-10-09
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

SERIES MCAXX (MODEL 851) ITE HEARING AID 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 1990-10-09 under 510(k) number K903583. The device is classified under product code ESD. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERIES MCAXX (MODEL 851) ITE HEARING AID?

SERIES MCAXX (MODEL 851) ITE HEARING AID is a medical device that received FDA 510(k) clearance on 1990-10-09. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K903583.

When did SERIES MCAXX (MODEL 851) ITE HEARING AID receive FDA 510(k) clearance?

SERIES MCAXX (MODEL 851) ITE HEARING AID received FDA 510(k) clearance on 1990-10-09, under 510(k) number K903583.

Who is the listed applicant for SERIES MCAXX (MODEL 851) ITE HEARING AID?

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 SERIES MCAXX (MODEL 851) ITE HEARING AID?

The FDA product code for SERIES MCAXX (MODEL 851) ITE HEARING AID is ESD.

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 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.

View all 58 devices →

Related Devices (Code: ESD)

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

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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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