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FDA 510(k)

PANASONIC WH-50 HEARING AID

K-Number: K833510 · 1983-11-14

Decision Date1983-11-14
Product CodeESD
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

PANASONIC WH-50 HEARING AID 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 1983-11-14 under 510(k) number K833510. 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 PANASONIC WH-50 HEARING AID?

PANASONIC WH-50 HEARING AID is a medical device that received FDA 510(k) clearance on 1983-11-14. The listed applicant is Panasonic Co. Div. Matsu Elec. Corp. America. The 510(k) number is K833510.

When did PANASONIC WH-50 HEARING AID receive FDA 510(k) clearance?

PANASONIC WH-50 HEARING AID received FDA 510(k) clearance on 1983-11-14, under 510(k) number K833510.

Who is the listed applicant for PANASONIC WH-50 HEARING AID?

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 PANASONIC WH-50 HEARING AID?

The FDA product code for PANASONIC WH-50 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 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

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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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