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FDA 510(k)

HEARING AID, UNITRON MODEL 975

K-Number: K781434 · 1978-08-31

Decision Date1978-08-31
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID, UNITRON MODEL 975 is the device name listed in this FDA 510(k) record. The listed applicant is Unitron Industries, Inc.. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K781434. 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, UNITRON MODEL 975?

HEARING AID, UNITRON MODEL 975 is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Unitron Industries, Inc.. The 510(k) number is K781434.

When did HEARING AID, UNITRON MODEL 975 receive FDA 510(k) clearance?

HEARING AID, UNITRON MODEL 975 received FDA 510(k) clearance on 1978-08-31, under 510(k) number K781434.

Who is the listed applicant for HEARING AID, UNITRON MODEL 975?

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

What is the FDA product code for HEARING AID, UNITRON MODEL 975?

The FDA product code for HEARING AID, UNITRON MODEL 975 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 Unitron Industries, 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.

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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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