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DIMENSION VISTA VITAMIN B12 AND FOLATE FLEX REAGENT CARTRIDGES AND LOCI 4 CALIBRATOR

K071224 Class II Traditional
Decision Date
2007-11-13
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K071224
Product Code CDD
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1810
Decision Date 2007-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIMENSION VISTA VITAMIN B12 AND FOLATE FLEX REAGENT CARTRIDGES AND LOCI 4 CALIBRATOR received FDA 510(k) clearance under submission number K071224, 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 2007-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code CDD and 21 CFR 862.1810, within the Clinical Chemistry review panel as a Class II device.