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DIMENSION VISTA MICROALBUMIN FLEX REAGENT CARTRIDGE; PROTEIN 3 CALIBRATOR; PROTEIN 3 CONTROL

K061990 Class II Traditional
Decision Date
2006-09-19
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K061990
Product Code DCF
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5040
Decision Date 2006-09-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIMENSION VISTA MICROALBUMIN FLEX REAGENT CARTRIDGE; PROTEIN 3 CALIBRATOR; PROTEIN 3 CONTROL received FDA 510(k) clearance under submission number K061990, sponsored by Dade Behring, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2006-09-19.

Classification & Regulation

This clearance is catalogued under FDA product code DCF and 21 CFR 866.5040, within the Immunology review panel as a Class II device.