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VITROS Chemistry Products hsCRP Reagent

K160712 Class II Traditional
Decision Date
2017-07-14
Sponsor / Applicant
Ortho Clinical Diagnostics

Technical Specification

510(k) Submission ID K160712
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2017-07-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

VITROS Chemistry Products hsCRP Reagent received FDA 510(k) clearance under submission number K160712, sponsored by Ortho Clinical Diagnostics. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2017-07-14.

Classification & Regulation

This clearance is catalogued under FDA product code DCK and 21 CFR 866.5270, within the Immunology review panel as a Class II device.