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PICCOLO C-REACTIVE PROTEIN (CRP) TEST SYSTEM

K091052 Class II Traditional
Decision Date
2010-01-15
Sponsor / Applicant
Abaxis, Inc.

Technical Specification

510(k) Submission ID K091052
Product Code DCN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2010-01-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PICCOLO C-REACTIVE PROTEIN (CRP) TEST SYSTEM received FDA 510(k) clearance under submission number K091052, sponsored by Abaxis, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2010-01-15.

Classification & Regulation

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