meddevicedb.com FDA Device Reference

SYMBIOS DISPOSABLE INFUSION PUMP KIT

K051474 Class II Special
Decision Date
2005-07-01
Sponsor / Applicant
Symbios Medical Products, LLC

Technical Specification

510(k) Submission ID K051474
Product Code MEB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2005-07-01
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYMBIOS DISPOSABLE INFUSION PUMP KIT received FDA 510(k) clearance under submission number K051474, sponsored by Symbios Medical Products, LLC. 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 2005-07-01.

Classification & Regulation

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