FDA PMA FDA Class 3 Approved 🇺🇸 United States

Pump, Infusion, Implanted, Programmable

PMA: P890055 · Supplement: S040 · Decision Jun 25, 2012
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Pump, Infusion, Implanted, Programmable
Trade Name
MEDSTREAM PROGRAMMABLE INFUSION SYSTEM
PMA Number
P890055
Supplement Number
S040
Device Class
FDA Class 3
Product Code
LKK
Generic Name
Pump, infusion, implanted, programmable
Medical Specialty
Unknown
Advisory Committee
General Hospital
Decision
Approved
Decision Code
APPR
Decision Date
June 25, 2012
Date Received
May 14, 2012
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR SOFTWARE MODIFICATIONS TO THE PROGRAMMABLE INFUSION SYSTEM. THESE MODIFICATIONS WERE DATA INTEGRITY CHECK IMPROVEMENT, RESOLUTION OF CONTROL UNIT KEYBOARD, FRAME CHECK SEQUENCE ALGORITHM UPGRADE, SOFTWARE ANOMALIES 015, 016, 017, 020 FIX, AND IMPROVEMENT OF THE BRIDGE BOLUS, PRIMING BOLUS AND SINGLE BOLUS PROCESSES.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LKK Pump, Infusion, Implanted, Programmable