meddevicedb.com FDA Device Reference

IV Fat Emulsion Administration Sets

K172544 Class II Special
Decision Date
2017-09-22
Sponsor / Applicant
Baxter Healthcare Corporation

Technical Specification

510(k) Submission ID K172544
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2017-09-22
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IV Fat Emulsion Administration Sets received FDA 510(k) clearance under submission number K172544, 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 2017-09-22.

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.