meddevicedb.com FDA Device Reference

MODIFICATION TO: HL168W TOUCH SCREEN

K013033 Class II Special
Decision Date
2001-10-23
Sponsor / Applicant
Health & Life Co., Ltd.

Technical Specification

510(k) Submission ID K013033
Product Code DXN
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1130
Decision Date 2001-10-23
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODIFICATION TO: HL168W TOUCH SCREEN received FDA 510(k) clearance under submission number K013033, sponsored by Health & Life Co., Ltd.. The device was reviewed via the Special premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2001-10-23.

Classification & Regulation

This clearance is catalogued under FDA product code DXN and 21 CFR 870.1130, within the Cardiovascular review panel as a Class II device.