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ACCESS OV MONITOR IMMUNOENZYMETRIC ASSAY

K023597 Class II Traditional
Decision Date
2002-12-11
Sponsor / Applicant
Beckman Coulter, Inc.

Technical Specification

510(k) Submission ID K023597
Product Code LTK
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.6010
Decision Date 2002-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACCESS OV MONITOR IMMUNOENZYMETRIC ASSAY received FDA 510(k) clearance under submission number K023597, 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 2002-12-11.

Classification & Regulation

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