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PHONAK 9100 SC-AF ITE HEARING INSTRUMENT

K911211 Class I Traditional
Decision Date
1991-04-17
Sponsor / Applicant
Phonak, Inc.

Technical Specification

510(k) Submission ID K911211
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1991-04-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHONAK 9100 SC-AF ITE HEARING INSTRUMENT received FDA 510(k) clearance under submission number K911211, sponsored by Phonak, Inc.. 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 1991-04-17.

Classification & Regulation

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