WIDEX HEARING AID #'S A12+T & A12+H— 510(k) K802307

Name: FDA 510(k) clearance K802307
Creator: U.S. Food and Drug Administration
Published: 1980-10-10

Substantially Equivalent

Hearing Aid Co.

FDA 510(k) clearance K802307 for WIDEX HEARING AID #'S A12+T & A12+H, Substantially Equivalent on 1980-10-10. Applicant: Hearing Aid Co.. Device class: 1.

Clearance details

Applicant: Hearing Aid Co.
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1980-09-23
Decision date: 1980-10-10
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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More clearances from Hearing Aid Co.

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K905784 — CUSTOM ITE HEARING AID1991-03-18
K881296 — HEARING AID (ALL-IN-THE-EAR)1988-04-12
K802306 — WIDEX HEARING AID #'S A18+T & A18+H1980-10-10

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