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FDA 510(k)

HEARING AID MODEL 8143

K-Number: K790270 · 1979-02-27

Decision Date1979-02-27
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID MODEL 8143 is the device name listed in this FDA 510(k) record. The listed applicant is Int'L Hearing Aids, Inc.. It received FDA 510(k) clearance on 1979-02-27 under 510(k) number K790270. 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 MODEL 8143?

HEARING AID MODEL 8143 is a medical device that received FDA 510(k) clearance on 1979-02-27. The listed applicant is Int'L Hearing Aids, Inc.. The 510(k) number is K790270.

When did HEARING AID MODEL 8143 receive FDA 510(k) clearance?

HEARING AID MODEL 8143 received FDA 510(k) clearance on 1979-02-27, under 510(k) number K790270.

Who is the listed applicant for HEARING AID MODEL 8143?

The FDA 510(k) record lists Int'L Hearing Aids, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEARING AID MODEL 8143?

The FDA product code for HEARING AID MODEL 8143 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 Int'L Hearing Aids, 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 21 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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