MODEL WHO1 HEARING AID— 510(k) K823285

Name: FDA 510(k) clearance K823285
Creator: U.S. Food and Drug Administration
Published: 1982-11-29

Substantially Equivalent

Panasonic Co. Div. Matsu Elec. Corp. America

FDA 510(k) clearance K823285 for MODEL WHO1 HEARING AID, Substantially Equivalent on 1982-11-29. Applicant: Panasonic Co. Div. Matsu Elec. Corp. America. Device class: 1.

Clearance details

Applicant: Panasonic Co. Div. Matsu Elec. Corp. America
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1982-11-04
Decision date: 1982-11-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.