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ECHO-OIL

K781631 Class I Traditional
Decision Date
1978-10-10
Sponsor / Applicant
Echo Laboratories, Inc.

Technical Specification

510(k) Submission ID K781631
Product Code EMX
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4100
Decision Date 1978-10-10
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ECHO-OIL received FDA 510(k) clearance under submission number K781631, sponsored by Echo Laboratories, 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 1978-10-10.

Classification & Regulation

This clearance is catalogued under FDA product code EMX and 21 CFR 874.4100, within the Ear, Nose, Throat review panel as a Class I device.