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FDA 510(k)

HEARING AID VARIOUS MODELS

K-Number: K821972 · 1982-07-20

Decision Date1982-07-20
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

HEARING AID VARIOUS MODELS is the device name listed in this FDA 510(k) record. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. It received FDA 510(k) clearance on 1982-07-20 under 510(k) number K821972. 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 VARIOUS MODELS?

HEARING AID VARIOUS MODELS is a medical device that received FDA 510(k) clearance on 1982-07-20. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. The 510(k) number is K821972.

When did HEARING AID VARIOUS MODELS receive FDA 510(k) clearance?

HEARING AID VARIOUS MODELS received FDA 510(k) clearance on 1982-07-20, under 510(k) number K821972.

Who is the listed applicant for HEARING AID VARIOUS MODELS?

The FDA 510(k) record lists Panasonic Co. Div. Matsu Elec. Corp. America as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HEARING AID VARIOUS MODELS?

The FDA product code for HEARING AID VARIOUS MODELS 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 Panasonic Co. Div. Matsu Elec. Corp. America 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.

View all 9 devices →

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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