FDA PMA FDA Class 3 Approved 🇺🇸 United States

Pump, Infusion, Implanted, Programmable

PMA: P800036 · Supplement: S036 · Decision Jun 23, 2006
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Pump, Infusion, Implanted, Programmable
Trade Name
INFUSAID MODEL 400 IMPLANTABLE INFUSION PUMP
PMA Number
P800036
Supplement Number
S036
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 23, 2006
Date Received
April 21, 2006
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Express GMP Supplement
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A MANUFACTURING SITE AT CODMAN & SHURTLEFF, INC.RAYNHAM, MASSACHUSETTS.

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