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ELECSYS CA 15-3 TEST SYSTEM

K001468 Class II Traditional
Decision Date
2000-10-23
Sponsor / Applicant
Roche Diagnostics Corp.

Technical Specification

510(k) Submission ID K001468
Product Code MOI
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.6010
Decision Date 2000-10-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ELECSYS CA 15-3 TEST SYSTEM received FDA 510(k) clearance under submission number K001468, sponsored by Roche Diagnostics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 2000-10-23.

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.