meddevicedb.com FDA Device Reference

MYOGLOBIN AND MYOGLOBIN CALIBRATORS ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL 973243, 973244

K021229 Class II Traditional
Decision Date
2002-06-28
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K021229
Product Code DDR
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5680
Decision Date 2002-06-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MYOGLOBIN AND MYOGLOBIN CALIBRATORS ON THE ACCESS IMMUNOASSAY SYSTEMS, MODEL 973243, 973244 received FDA 510(k) clearance under submission number K021229, sponsored by Beckman Coulter, 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 2002-06-28.

Classification & Regulation

This clearance is catalogued under FDA product code DDR and 21 CFR 866.5680, within the Immunology review panel as a Class II device.