meddevicedb.com FDA Device Reference

BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061

K001022 Class II Traditional
Decision Date
2000-09-26
Sponsor / Applicant
Biocheck, Inc.

Technical Specification

510(k) Submission ID K001022
Product Code JZG
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5630
Decision Date 2000-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

BIOCHECK, INC. B-2 MICROGLOBIN ENZYME IMMUNOASAY TEST KIT, MODEL BC-1061 received FDA 510(k) clearance under submission number K001022, 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 2000-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code JZG and 21 CFR 866.5630, within the Immunology review panel as a Class II device.