DOCE ALL-IN-THE-EAR AID— 510(k) K822817

Name: FDA 510(k) clearance K822817
Creator: U.S. Food and Drug Administration
Published: 1983-01-18

Substantially Equivalent

Fidelty Hearing Instruments, Inc.

FDA 510(k) clearance K822817 for DOCE ALL-IN-THE-EAR AID, Substantially Equivalent on 1983-01-18. Applicant: Fidelty Hearing Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Fidelty Hearing Instruments, Inc.
Product code: Code FSD
Device class: Class 1
Regulation: 21 CFR 880.5160
Advisory panel: General Hospital
Date received: 1982-09-20
Decision date: 1983-01-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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