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FDA 510(k)

HEARING AID (ALL-IN-THE-EAR)

K-Number: K874218 · 1987-12-11

Decision Date1987-12-11
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID (ALL-IN-THE-EAR) is the device name listed in this FDA 510(k) record. The listed applicant is Audiology & Hearing Aid Clinic. It received FDA 510(k) clearance on 1987-12-11 under 510(k) number K874218. 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 HEARING AID (ALL-IN-THE-EAR)?

HEARING AID (ALL-IN-THE-EAR) is a medical device that received FDA 510(k) clearance on 1987-12-11. The listed applicant is Audiology & Hearing Aid Clinic. The 510(k) number is K874218.

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

HEARING AID (ALL-IN-THE-EAR) received FDA 510(k) clearance on 1987-12-11, under 510(k) number K874218.

Who is the listed applicant for HEARING AID (ALL-IN-THE-EAR)?

The FDA 510(k) record lists Audiology & Hearing Aid Clinic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEARING AID (ALL-IN-THE-EAR)?

The FDA product code for HEARING AID (ALL-IN-THE-EAR) 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.

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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