meddevicedb.com FDA Device Reference

ACCESS CEA REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL 33200, 33205, 33206 & 33209

K981985 Class II Traditional
Decision Date
1998-09-24
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K981985
Product Code DHX
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.6010
Decision Date 1998-09-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCESS CEA REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL 33200, 33205, 33206 & 33209 received FDA 510(k) clearance under submission number K981985, 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 1998-09-24.

Classification & Regulation

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