Cleared Traditional

K790745 - _MODEL WC-1 BEHIND-THE-EAR HEARING AID (FDA 510(k) Clearance)

May 1979
Decision
15d
Days
Class 1
Risk

K790745 is an FDA 510(k) clearance for the _MODEL WC-1 BEHIND-THE-EAR HEARING AID. This device is classified as a Hearing Aid, Air-conduction, Prescription (Class I - General Controls, product code ESD).

Submitted by Starkey Laboratories, Inc. (Mchenry, US). The FDA issued a Cleared decision on May 1, 1979, 15 days after receiving the submission on April 16, 1979.

This device falls under the Ear, Nose, Throat FDA review panel. Regulated under 21 CFR 874.3300. An Air-conduction Hearing Aid Is A Wearable Sound Amplifying Device Intended To Compensate For Impaired Hearing That Conducts Sound To The Ear Through The Air. This Is A Prescription Hearing Aid..

Submission Details

510(k) Number K790745 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received April 16, 1979
Decision Date May 01, 1979
Days to Decision 15 days
Submission Type Traditional
Review Panel Ear, Nose, Throat (EN)
Summary -

Device Classification

Product Code ESD - Hearing Aid, Air-conduction, Prescription
Device Class Class I - General Controls
CFR Regulation 21 CFR 874.3300
Definition An Air-conduction Hearing Aid Is A Wearable Sound Amplifying Device Intended To Compensate For Impaired Hearing That Conducts Sound To The Ear Through The Air. This Is A Prescription Hearing Aid.