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FDA 510(k)

HEARING AID (IN-THE-EAR)

K-Number: K873070 · 1987-09-15

Decision Date1987-09-15
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID (IN-THE-EAR) is the device name listed in this FDA 510(k) record. The listed applicant is Central Illinois Hearing Aid Centers, Inc.. It received FDA 510(k) clearance on 1987-09-15 under 510(k) number K873070. 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 (IN-THE-EAR)?

HEARING AID (IN-THE-EAR) is a medical device that received FDA 510(k) clearance on 1987-09-15. The listed applicant is Central Illinois Hearing Aid Centers, Inc.. The 510(k) number is K873070.

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

HEARING AID (IN-THE-EAR) received FDA 510(k) clearance on 1987-09-15, under 510(k) number K873070.

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

The FDA 510(k) record lists Central Illinois Hearing Aid Centers, Inc. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for HEARING AID (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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