meddevicedb.com FDA Device Reference

DIMENSION VISTA SYSTEM IGG FLEX REAGENT CARTRIDGE, DIMENSION VISTA SYSTEM PROTEIN 1 CALIBRATOR, AND DIMENSION VISTA SYST

K081161 Class II Traditional
Decision Date
2008-07-28
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K081161
Product Code CFN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5510
Decision Date 2008-07-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIMENSION VISTA SYSTEM IGG FLEX REAGENT CARTRIDGE, DIMENSION VISTA SYSTEM PROTEIN 1 CALIBRATOR, AND DIMENSION VISTA SYST received FDA 510(k) clearance under submission number K081161, 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 2008-07-28.

Classification & Regulation

This clearance is catalogued under FDA product code CFN and 21 CFR 866.5510, within the Immunology review panel as a Class II device.