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PHONIC EAR

K780936 Class II Traditional
Decision Date
1978-06-22
Sponsor / Applicant
Hc Electronics

Technical Specification

510(k) Submission ID K780936
Product Code EPF
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3320
Decision Date 1978-06-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHONIC EAR received FDA 510(k) clearance under submission number K780936, sponsored by Hc Electronics. 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 1978-06-22.

Classification & Regulation

This clearance is catalogued under FDA product code EPF and 21 CFR 874.3320, within the Ear, Nose, Throat review panel as a Class II device.