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CRP-ADVANCE ASSAY, MODELS 250-20, 250-25

K060139 Class II Traditional
Decision Date
2006-04-28
Sponsor / Applicant
Diagnostic Chemicals , Ltd.

Technical Specification

510(k) Submission ID K060139
Product Code DCK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2006-04-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRP-ADVANCE ASSAY, MODELS 250-20, 250-25 received FDA 510(k) clearance under submission number K060139, sponsored by Diagnostic Chemicals , Ltd.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2006-04-28.

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.