meddevicedb.com FDA Device Reference

Blood Administration Sets

K220558 Class II Traditional
Decision Date
2022-11-17
Sponsor / Applicant
Baxter Healthcare Corporation

Technical Specification

510(k) Submission ID K220558
Product Code BRZ
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2022-11-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Blood Administration Sets received FDA 510(k) clearance under submission number K220558, sponsored by Baxter Healthcare Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2022-11-17.

Classification & Regulation

This clearance is catalogued under FDA product code BRZ and 21 CFR 880.5440, within the General Hospital review panel as a Class II device.