meddevicedb.com FDA Device Reference

ITE MODEL ADOBE 100 FULL CUSTOM

K931590 Class I Traditional
Decision Date
1993-05-19
Sponsor / Applicant
Widex Hearing Aid Co., Inc.

Technical Specification

510(k) Submission ID K931590
Product Code ESD
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.3300
Decision Date 1993-05-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ITE MODEL ADOBE 100 FULL CUSTOM received FDA 510(k) clearance under submission number K931590, sponsored by Widex Hearing Aid Co., 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 1993-05-19.

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.