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AUDIOSCAN

K926336 Class II Traditional
Decision Date
1993-03-04
Sponsor / Applicant
Electrocaine Medical System

Technical Specification

510(k) Submission ID K926336
Product Code EWO
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.1050
Decision Date 1993-03-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AUDIOSCAN received FDA 510(k) clearance under submission number K926336, sponsored by Electrocaine Medical System. 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 1993-03-04.

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.