meddevicedb.com FDA Device Reference

TD-4277 BLOOD GLUCOSE MONITORING SYSTEM, MODEL 4277

K100322 Class II Traditional
Decision Date
2010-06-28
Sponsor / Applicant
Taidoc Technology Corporation

Technical Specification

510(k) Submission ID K100322
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2010-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TD-4277 BLOOD GLUCOSE MONITORING SYSTEM, MODEL 4277 received FDA 510(k) clearance under submission number K100322, sponsored by Taidoc Technology Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2010-06-28.

Classification & Regulation

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