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BIOCHECK CARDIAC-1 CRP RAPID TEST, MODEL BC-804114

K040030 Class II Traditional
Decision Date
2004-06-16
Sponsor / Applicant
Biocheck, Inc.

Technical Specification

510(k) Submission ID K040030
Product Code DCN
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5270
Decision Date 2004-06-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOCHECK CARDIAC-1 CRP RAPID TEST, MODEL BC-804114 received FDA 510(k) clearance under submission number K040030, sponsored by Biocheck, 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 2004-06-16.

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.