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DIAZYME HS CRP ASSAY KIT / CALIBRATOR SET / CONTROL SET

K103557 Class II Traditional
Decision Date
2011-04-27
Sponsor / Applicant
Diazyme Laboratories

Technical Specification

510(k) Submission ID K103557
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2011-04-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DIAZYME HS CRP ASSAY KIT / CALIBRATOR SET / CONTROL SET received FDA 510(k) clearance under submission number K103557, sponsored by Diazyme Laboratories. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2011-04-27.

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.