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FDA 510(k)

MICRO-EAR CANAL IN-THE-EAR HEARING AID

K-Number: K870079 · 1987-03-03

Decision Date1987-03-03
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MICRO-EAR CANAL IN-THE-EAR HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Ear Hearing Center, Inc.. It received FDA 510(k) clearance on 1987-03-03 under 510(k) number K870079. 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 MICRO-EAR CANAL IN-THE-EAR HEARING AID?

MICRO-EAR CANAL IN-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1987-03-03. The listed applicant is Micro-Ear Hearing Center, Inc.. The 510(k) number is K870079.

When did MICRO-EAR CANAL IN-THE-EAR HEARING AID receive FDA 510(k) clearance?

MICRO-EAR CANAL IN-THE-EAR HEARING AID received FDA 510(k) clearance on 1987-03-03, under 510(k) number K870079.

Who is the listed applicant for MICRO-EAR CANAL IN-THE-EAR HEARING AID?

The FDA 510(k) record lists Micro-Ear Hearing Center, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICRO-EAR CANAL IN-THE-EAR HEARING AID?

The FDA product code for MICRO-EAR CANAL IN-THE-EAR 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 Micro-Ear Hearing Center, 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.

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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