meddevicedb.com FDA Device Reference

IV Administration Set

K213778 Class II Traditional
Decision Date
2022-03-03
Sponsor / Applicant
B.Braun Medical, Inc.

Technical Specification

510(k) Submission ID K213778
Product Code FPA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5440
Decision Date 2022-03-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

IV Administration Set received FDA 510(k) clearance under submission number K213778, sponsored by B.Braun Medical, Inc.. 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 2022-03-03.

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.