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FDA 510(k)

ACCUTONE IN-THE-EAR HEARING AID

K-Number: K881193 · 1988-05-18

Decision Date1988-05-18
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ACCUTONE IN-THE-EAR HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Interstate Hearing Aid Service. It received FDA 510(k) clearance on 1988-05-18 under 510(k) number K881193. 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 ACCUTONE IN-THE-EAR HEARING AID?

ACCUTONE IN-THE-EAR HEARING AID is a medical device that received FDA 510(k) clearance on 1988-05-18. The listed applicant is Interstate Hearing Aid Service. The 510(k) number is K881193.

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

ACCUTONE IN-THE-EAR HEARING AID received FDA 510(k) clearance on 1988-05-18, under 510(k) number K881193.

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

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

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

The FDA product code for ACCUTONE 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.

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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