meddevicedb.com FDA Device Reference

DIMENSION VISTA INTEGRATED SYSTEM

K051087 Class I Traditional
Decision Date
2005-07-11
Sponsor / Applicant
Dade Behring, Inc.

Technical Specification

510(k) Submission ID K051087
Product Code JJE
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.2160
Decision Date 2005-07-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIMENSION VISTA INTEGRATED SYSTEM received FDA 510(k) clearance under submission number K051087, 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 2005-07-11.

Classification & Regulation

This clearance is catalogued under FDA product code JJE and 21 CFR 862.2160, within the Clinical Chemistry review panel as a Class I device.