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DUAL CHAMBER TPN CONTAINER

K073538 Class II Traditional
Decision Date
2008-03-12
Sponsor / Applicant
B.Braun Medical, Inc.

Technical Specification

510(k) Submission ID K073538
Product Code KPE
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5025
Decision Date 2008-03-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DUAL CHAMBER TPN CONTAINER received FDA 510(k) clearance under submission number K073538, 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 2008-03-12.

Classification & Regulation

This clearance is catalogued under FDA product code KPE and 21 CFR 880.5025, within the General Hospital review panel as a Class II device.