SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT— 510(k) K901388

Substantially Equivalent

Miracle-Ear, Inc.

FDA 510(k) clearance K901388 for SEARS MODEL LM9091 IN-THE-EAR HEARING INSTRUMENT, Substantially Equivalent on 1990-04-16. Applicant: Miracle-Ear, Inc..

Clearance details

Applicant: Miracle-Ear, Inc.
Product code: Code ESD
Advisory panel: Ear, Nose, Throat
Date received: 1990-03-26
Decision date: 1990-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Golden Valley, MN, US

Download summary PDF View on FDA.gov ↗

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