meddevicedb.com FDA Device Reference

TS3 TUBING SET

K031151 Class II Traditional
Decision Date
2003-06-26
Sponsor / Applicant
Global Blood Resources, LLC

Technical Specification

510(k) Submission ID K031151
Product Code DWF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4210
Decision Date 2003-06-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TS3 TUBING SET received FDA 510(k) clearance under submission number K031151, sponsored by Global Blood Resources, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2003-06-26.

Classification & Regulation

This clearance is catalogued under FDA product code DWF and 21 CFR 870.4210, within the Cardiovascular review panel as a Class II device.