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FDA 510(k)

MODEL WC-3 HEARING AID

K-Number: K790651 · 1979-04-10

Decision Date1979-04-10
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

MODEL WC-3 HEARING AID 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 1979-04-10 under 510(k) number K790651. 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 MODEL WC-3 HEARING AID?

MODEL WC-3 HEARING AID is a medical device that received FDA 510(k) clearance on 1979-04-10. The listed applicant is Starkey Laboratories, Inc.. The 510(k) number is K790651.

When did MODEL WC-3 HEARING AID receive FDA 510(k) clearance?

MODEL WC-3 HEARING AID received FDA 510(k) clearance on 1979-04-10, under 510(k) number K790651.

Who is the listed applicant for MODEL WC-3 HEARING AID?

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 MODEL WC-3 HEARING AID?

The FDA product code for MODEL WC-3 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.

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

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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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