HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANAL— 510(k) K963607

Name: FDA 510(k) clearance K963607
Creator: U.S. Food and Drug Administration
Published: 1996-09-20

Substantially Equivalent

Midwest City Hearing Aid Center

FDA 510(k) clearance K963607 for HORIZON 1 AND 2 PROGRAMABLE FULL SHELL AND IN THE CANAL, Substantially Equivalent on 1996-09-20. Applicant: Midwest City Hearing Aid Center. Device class: 1.

Clearance details

Applicant: Midwest City Hearing Aid Center
Product code: Code ESD
Device class: Class 1
Regulation: 21 CFR 874.3300
Advisory panel: Ear, Nose, Throat
Date received: 1996-09-09
Decision date: 1996-09-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Midwest City, OK, US

Download summary PDF View on FDA.gov ↗

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