meddevicedb.com FDA Device Reference

HOME CARE EAR EXAMINATIO KIT

K944897 Class I Traditional
Decision Date
1994-11-08
Sponsor / Applicant
Home Care Instruments, Inc.

Technical Specification

510(k) Submission ID K944897
Product Code ERA
Medical Specialty / Panel Ear, Nose, Throat
Regulation Citation 21 CFR 874.4770
Decision Date 1994-11-08
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HOME CARE EAR EXAMINATIO KIT received FDA 510(k) clearance under submission number K944897, sponsored by Home Care Instruments, 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 1994-11-08.

Classification & Regulation

This clearance is catalogued under FDA product code ERA and 21 CFR 874.4770, within the Ear, Nose, Throat review panel as a Class I device.