FDA PMA FDA Class 3 Approved 🇺🇸 United States

Pump, Infusion, Implanted, Programmable

PMA: P890055 · Supplement: S030 · Decision Mar 15, 2011
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
S030
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
March 15, 2011
Date Received
January 18, 2011
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Postapproval Study Protocol - OSB
Expedited Review
N

Advisory Committee Statement

APPROVAL OF THE POST-APPROVAL PROTOCOL.

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