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INTERACOUSTICS MODEL MT 10, HANDHELD IMPEDANCE AUDIOMETER

K983832 Class II Traditional
Decision Date
1999-01-25
Sponsor / Applicant
Idem (Int'L Dist. of Electronics For Medicine)

Technical Specification

510(k) Submission ID K983832
Product Code ETY
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1090
Decision Date 1999-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INTERACOUSTICS MODEL MT 10, HANDHELD IMPEDANCE AUDIOMETER received FDA 510(k) clearance under submission number K983832, sponsored by Idem (Int'L Dist. of Electronics For Medicine). 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 1999-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code ETY and 21 CFR 874.1090, within the Ear, Nose, Throat review panel as a Class II device.