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ACCESS IMMUNOASSAY SYSTEMS BR MONITOR, AND CALIBRATORS, MODEL(S) 387620,AND 387647

K072612 Class II Special
Decision Date
2007-10-26
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K072612
Product Code MOI
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.6010
Decision Date 2007-10-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCESS IMMUNOASSAY SYSTEMS BR MONITOR, AND CALIBRATORS, MODEL(S) 387620,AND 387647 received FDA 510(k) clearance under submission number K072612, sponsored by Beckman Coulter, Inc.. The device was reviewed via the Special premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2007-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code MOI and 21 CFR 866.6010, within the Immunology review panel as a Class II device.