MIRACLE EAR MODEL CK IN-THE-EAR HEARING AID— 510(k) K900050

Substantially Equivalent

Miracle-Ear, Inc.

FDA 510(k) clearance K900050 for MIRACLE EAR MODEL CK IN-THE-EAR HEARING AID, Substantially Equivalent on 1990-03-14. Applicant: Miracle-Ear, Inc..

Clearance details

Applicant: Miracle-Ear, Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1990-01-03
Decision date: 1990-03-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Minneapolis, MN, US

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