meddevicedb.com FDA Device Reference

Solution Administration Sets with 0.2 Micron Filter

K153158 Class II Special
Decision Date
2015-12-28
Sponsor / Applicant
Baxter Healthcare Corporation

Technical Specification

510(k) Submission ID K153158
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2015-12-28
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Solution Administration Sets with 0.2 Micron Filter received FDA 510(k) clearance under submission number K153158, sponsored by Baxter Healthcare Corporation. The device was reviewed via the Special premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2015-12-28.

Classification & Regulation

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