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FDA 510(k)

ITE TYPE HEARING AID ABS MODEL

K-Number: K880938 · 1988-05-13

Decision Date1988-05-13
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ITE TYPE HEARING AID ABS MODEL is the device name listed in this FDA 510(k) record. The listed applicant is A Better Sound Corp.. It received FDA 510(k) clearance on 1988-05-13 under 510(k) number K880938. 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 ITE TYPE HEARING AID ABS MODEL?

ITE TYPE HEARING AID ABS MODEL is a medical device that received FDA 510(k) clearance on 1988-05-13. The listed applicant is A Better Sound Corp.. The 510(k) number is K880938.

When did ITE TYPE HEARING AID ABS MODEL receive FDA 510(k) clearance?

ITE TYPE HEARING AID ABS MODEL received FDA 510(k) clearance on 1988-05-13, under 510(k) number K880938.

Who is the listed applicant for ITE TYPE HEARING AID ABS MODEL?

The FDA 510(k) record lists A Better Sound Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ITE TYPE HEARING AID ABS MODEL?

The FDA product code for ITE TYPE HEARING AID ABS MODEL 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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