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FDA 510(k)

HEARING AID MODEL E1-P

K-Number: K811285 · 1981-06-16

Decision Date1981-06-16
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID MODEL E1-P 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 1981-06-16 under 510(k) number K811285. 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 E1-P?

HEARING AID MODEL E1-P is a medical device that received FDA 510(k) clearance on 1981-06-16. The listed applicant is Unitron Industries, Inc.. The 510(k) number is K811285.

When did HEARING AID MODEL E1-P receive FDA 510(k) clearance?

HEARING AID MODEL E1-P received FDA 510(k) clearance on 1981-06-16, under 510(k) number K811285.

Who is the listed applicant for HEARING AID MODEL E1-P?

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 MODEL E1-P?

The FDA product code for HEARING AID MODEL E1-P 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

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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