meddevicedb.com FDA Device Reference

CRESTLINE CB BEHIND-THE-EAR HEARING AID

K850981 Class I Traditional
Decision Date
1985-05-31
Sponsor / Applicant
Dahlberg Electronics, Inc.

Technical Specification

510(k) Submission ID K850981
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1985-05-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRESTLINE CB BEHIND-THE-EAR HEARING AID received FDA 510(k) clearance under submission number K850981, sponsored by Dahlberg Electronics, 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 1985-05-31.

Classification & Regulation

This clearance is catalogued under FDA product code ESD and 21 CFR 874.3300, within the Ear, Nose, Throat review panel as a Class I device.