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FDA 510(k)

CUSTOM IN-THE-EAR HEARING AID SERIES MCA20

K-Number: K873468 · 1987-09-29

Decision Date1987-09-29
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

CUSTOM IN-THE-EAR HEARING AID SERIES MCA20 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 1987-09-29 under 510(k) number K873468. 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 CUSTOM IN-THE-EAR HEARING AID SERIES MCA20?

CUSTOM IN-THE-EAR HEARING AID SERIES MCA20 is a medical device that received FDA 510(k) clearance on 1987-09-29. The listed applicant is Maico Hearing Instruments, Inc.. The 510(k) number is K873468.

When did CUSTOM IN-THE-EAR HEARING AID SERIES MCA20 receive FDA 510(k) clearance?

CUSTOM IN-THE-EAR HEARING AID SERIES MCA20 received FDA 510(k) clearance on 1987-09-29, under 510(k) number K873468.

Who is the listed applicant for CUSTOM IN-THE-EAR HEARING AID SERIES MCA20?

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 CUSTOM IN-THE-EAR HEARING AID SERIES MCA20?

The FDA product code for CUSTOM IN-THE-EAR HEARING AID SERIES MCA20 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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