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FDA 510(k)

HEARING AID-MODEL PE-1

K-Number: K772101 · 1977-11-21

Decision Date1977-11-21
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID-MODEL PE-1 is the device name listed in this FDA 510(k) record. The listed applicant is Starkey Laboratories, Inc.. It received FDA 510(k) clearance on 1977-11-21 under 510(k) number K772101. 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 PE-1?

HEARING AID-MODEL PE-1 is a medical device that received FDA 510(k) clearance on 1977-11-21. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K772101.

When did HEARING AID-MODEL PE-1 receive FDA 510(k) clearance?

HEARING AID-MODEL PE-1 received FDA 510(k) clearance on 1977-11-21, under 510(k) number K772101.

Who is the listed applicant for HEARING AID-MODEL PE-1?

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

What is the FDA product code for HEARING AID-MODEL PE-1?

The FDA product code for HEARING AID-MODEL PE-1 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 Starkey Laboratories, 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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