EYEGLASS HEARING AID— 510(k) K760609

Name: FDA 510(k) clearance K760609
Creator: U.S. Food and Drug Administration
Published: 1976-09-21

Substantially Equivalent

Zenith Hearing Instrument Co.

FDA 510(k) clearance K760609 for EYEGLASS HEARING AID, Substantially Equivalent on 1976-09-21. Applicant: Zenith Hearing Instrument Co.. Device class: 1.

Clearance details

Applicant: Zenith Hearing Instrument Co.
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1976-09-09
Decision date: 1976-09-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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