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MIDDLE EAR ANALYZER (IMPED. AUDIOMTR)

K790846 Class II Traditional
Decision Date
1979-05-17
Sponsor / Applicant
Grason-Stadler, Inc.

Technical Specification

510(k) Submission ID K790846
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1979-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MIDDLE EAR ANALYZER (IMPED. AUDIOMTR) received FDA 510(k) clearance under submission number K790846, sponsored by Grason-Stadler, 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 1979-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code EWO and 21 CFR 874.1050, within the Ear, Nose, Throat review panel as a Class II device.