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CHROMALEX RHEUMATOID FACTOR LATEX TEST SYSTEM

K953261 Class II Traditional
Decision Date
1995-08-15
Sponsor / Applicant
Shared Systems, Inc.

Technical Specification

510(k) Submission ID K953261
Product Code DHR
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5775
Decision Date 1995-08-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CHROMALEX RHEUMATOID FACTOR LATEX TEST SYSTEM received FDA 510(k) clearance under submission number K953261, sponsored by Shared Systems, 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 1995-08-15.

Classification & Regulation

This clearance is catalogued under FDA product code DHR and 21 CFR 866.5775, within the Immunology review panel as a Class II device.