meddevicedb.com FDA Device Reference

BIOMETER AUDIOMETER

K883505 Class II Traditional
Decision Date
1989-08-21
Sponsor / Applicant
Micro Audiometrics Corp.

Technical Specification

510(k) Submission ID K883505
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1989-08-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOMETER AUDIOMETER received FDA 510(k) clearance under submission number K883505, sponsored by Micro Audiometrics Corp.. 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 1989-08-21.

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.