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FDA 510(k)

ALPHA MODEL I ITE HEARING AID

K-Number: K890271 · 1989-06-16

Decision Date1989-06-16
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ALPHA MODEL I ITE HEARING AID is the device name listed in this FDA 510(k) record. The listed applicant is Alpha Instruments, Inc.. It received FDA 510(k) clearance on 1989-06-16 under 510(k) number K890271. 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 ALPHA MODEL I ITE HEARING AID?

ALPHA MODEL I ITE HEARING AID is a medical device that received FDA 510(k) clearance on 1989-06-16. The listed applicant is Alpha Instruments, Inc.. The 510(k) number is K890271.

When did ALPHA MODEL I ITE HEARING AID receive FDA 510(k) clearance?

ALPHA MODEL I ITE HEARING AID received FDA 510(k) clearance on 1989-06-16, under 510(k) number K890271.

Who is the listed applicant for ALPHA MODEL I ITE HEARING AID?

The FDA 510(k) record lists Alpha Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALPHA MODEL I ITE HEARING AID?

The FDA product code for ALPHA MODEL I ITE 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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