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DIMENSION VISTA SYSTEM BILIRUBIN CALIBRATOR, MODEL KC210

K072717 Class II Traditional
Decision Date
2007-12-12
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K072717
Product Code JIT
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2007-12-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIMENSION VISTA SYSTEM BILIRUBIN CALIBRATOR, MODEL KC210 received FDA 510(k) clearance under submission number K072717, sponsored by Dade Behring, Inc.. 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 2007-12-12.

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.