meddevicedb.com FDA Device Reference

RHEUMATOID FACTOR TEST SYSTEMS

K802688 Class II Traditional
Decision Date
1980-12-18
Sponsor / Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic

Technical Specification

510(k) Submission ID K802688
Product Code DHR
Medical Specialty / Panel Immunology
Regulation Citation 21 CFR 866.5775
Decision Date 1980-12-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

RHEUMATOID FACTOR TEST SYSTEMS received FDA 510(k) clearance under submission number K802688, sponsored by Bd Becton Dickinson Vacutainer Systems Preanalytic. The device was reviewed via the Traditional premarket notification pathway and assigned to the Immunology review panel. The statutory decision date of record is 1980-12-18.

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.