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AUDINA PREWIRES (FACEPLATE HEARING AID SERIES)

K942236 Class I Traditional
Decision Date
1994-06-17
Sponsor / Applicant
Audina Hearing Instrument

Technical Specification

510(k) Submission ID K942236
Product Code LRB
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1994-06-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUDINA PREWIRES (FACEPLATE HEARING AID SERIES) received FDA 510(k) clearance under submission number K942236, sponsored by Audina Hearing Instrument. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ear, Nose, Throat review panel. The statutory decision date of record is 1994-06-17.

Classification & Regulation

This clearance is catalogued under FDA product code LRB and 21 CFR 874.3300, within the Ear, Nose, Throat review panel as a Class I device.