meddevicedb.com FDA Device Reference

ONE TOUCH ULTRA BLOOD GLUCOSE MONITORING SYSTEM

K002134 Class II Special
Decision Date
2000-08-07
Sponsor / Applicant
Selfcare, Inc.

Technical Specification

510(k) Submission ID K002134
Product Code CGA
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2000-08-07
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ONE TOUCH ULTRA BLOOD GLUCOSE MONITORING SYSTEM received FDA 510(k) clearance under submission number K002134, sponsored by Selfcare, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2000-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code CGA and 21 CFR 862.1345, within the Clinical Chemistry review panel as a Class II device.