meddevicedb.com FDA Device Reference

ADVIA CHEMISTRY DRUG CALIBRATOR I MODEL 10376770

K093732 Class II Abbreviated
Decision Date
2010-03-22
Sponsor / Applicant
Siemens Healthcare Diagnostics

Technical Specification

510(k) Submission ID K093732
Product Code JIX
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1150
Decision Date 2010-03-22
Clearance Pathway Abbreviated

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVIA CHEMISTRY DRUG CALIBRATOR I MODEL 10376770 received FDA 510(k) clearance under submission number K093732, sponsored by Siemens Healthcare Diagnostics. The device was reviewed via the Abbreviated premarket notification pathway and assigned to the Clinical Chemistry review panel. The statutory decision date of record is 2010-03-22.

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.