meddevicedb.com FDA Device Reference

ASCENSIA DEX 2 DIABETES CARE SYSTEM

K023584 Class II Special
Decision Date
2002-11-20
Sponsor / Applicant
Bayer Corp.

Technical Specification

510(k) Submission ID K023584
Product Code NBW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1345
Decision Date 2002-11-20
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASCENSIA DEX 2 DIABETES CARE SYSTEM received FDA 510(k) clearance under submission number K023584, sponsored by Bayer Corp.. 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 2002-11-20.

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.