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ADVIA Centaur Intact Parathyroid Hormone (PTH) Assay

K163658 Class II Traditional
Decision Date
2017-05-23
Sponsor / Applicant
Siemens Healthcare Diagnostics, Inc.

Technical Specification

510(k) Submission ID K163658
Product Code CEW
Medical Specialty / Panel Clinical Chemistry
Regulation Citation 21 CFR 862.1545
Decision Date 2017-05-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADVIA Centaur Intact Parathyroid Hormone (PTH) Assay received FDA 510(k) clearance under submission number K163658, sponsored by Siemens Healthcare Diagnostics, 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 2017-05-23.

Classification & Regulation

This clearance is catalogued under FDA product code CEW and 21 CFR 862.1545, within the Clinical Chemistry review panel as a Class II device.