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ADVIA CANTAUR AND ACS:180 INSULIN CALIBRATOR

K021535 Class II Traditional
Decision Date
2002-06-27
Sponsor / Applicant
Bayer Diagnostics Corp.

Technical Specification

510(k) Submission ID K021535
Product Code JIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2002-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVIA CANTAUR AND ACS:180 INSULIN CALIBRATOR received FDA 510(k) clearance under submission number K021535, sponsored by Bayer Diagnostics Corp.. 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 2002-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code JIT and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.