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ADVIA CHEMISTRY FRUCTOSAMINE ASSAY, ADVIA CHEMISTRY FRUCTOSAMINE CALIBRATOR

K131307 Class II Traditional
Decision Date
2014-01-24
Sponsor / Applicant
Siemens Healthcare Diagnostics, Inc.

Technical Specification

510(k) Submission ID K131307
Product Code LCP
Medical Specialty / Panel Hematology
Regulation Citation 21 CFR 864.7470
Decision Date 2014-01-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVIA CHEMISTRY FRUCTOSAMINE ASSAY, ADVIA CHEMISTRY FRUCTOSAMINE CALIBRATOR received FDA 510(k) clearance under submission number K131307, sponsored by Siemens Healthcare Diagnostics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Hematology review panel. The statutory decision date of record is 2014-01-24.

Classification & Regulation

This clearance is catalogued under FDA product code LCP and 21 CFR 864.7470, within the Hematology review panel as a Class II device.