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HEARTLAND TECHNOLOGIES, ITE, ITC, CIC

K971845 Class I Traditional
Decision Date
1997-08-15
Sponsor / Applicant
Sound Hearing Instruments, Inc.

Technical Specification

510(k) Submission ID K971845
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1997-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEARTLAND TECHNOLOGIES, ITE, ITC, CIC received FDA 510(k) clearance under submission number K971845, sponsored by Sound Hearing Instruments, 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 1997-08-15.

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.