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DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM

K072921 Class II Special
Decision Date
2007-11-26
Sponsor / Applicant
Symbios Medical Products, LLC

Technical Specification

510(k) Submission ID K072921
Product Code MEB
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5725
Decision Date 2007-11-26
Clearance Pathway Special

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE INFUSION PUMP KIT, GO PUMP RAPID RECOVERY SYSTEM received FDA 510(k) clearance under submission number K072921, 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 2007-11-26.

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.