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DIMENSION CHEMISTRY III CALIBRATORY

K123321 Class II Traditional
Decision Date
2013-02-15
Sponsor / Applicant
Siemens Healthcare Diagnostics

Technical Specification

510(k) Submission ID K123321
Product Code JIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2013-02-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIMENSION CHEMISTRY III CALIBRATORY received FDA 510(k) clearance under submission number K123321, sponsored by Siemens Healthcare Diagnostics. 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 2013-02-15.

Classification & Regulation

This clearance is catalogued under FDA product code JIX and 21 CFR 862.1150, within the Clinical Chemistry review panel as a Class II device.