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PERFUSOR SPACE INFUSION SYRINGE PUMP SYSTEM

K092313 Class II Traditional
Decision Date
2009-11-04
Sponsor / Applicant
B.Braun Medical, Inc.

Technical Specification

510(k) Submission ID K092313
Product Code MEA
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2009-11-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PERFUSOR SPACE INFUSION SYRINGE PUMP SYSTEM received FDA 510(k) clearance under submission number K092313, 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 2009-11-04.

Classification & Regulation

This clearance is catalogued under FDA product code MEA and 21 CFR 880.5725, within the General Hospital review panel as a Class II device.