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ACCESS THYROGLOBULIN ANTIBODY AND CALIBRATORS ON THE ACCESS IMMUNOASSAY SYSTEMS, MODELS 33890, 33895

K012208 Class II Traditional
Decision Date
2001-09-07
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K012208
Product Code DDC
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5870
Decision Date 2001-09-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCESS THYROGLOBULIN ANTIBODY AND CALIBRATORS ON THE ACCESS IMMUNOASSAY SYSTEMS, MODELS 33890, 33895 received FDA 510(k) clearance under submission number K012208, 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 2001-09-07.

Classification & Regulation

This clearance is catalogued under FDA product code DDC and 21 CFR 866.5870, within the Immunology review panel as a Class II device.