FDA PMA FDA Class 3 Approved 🇺🇸 United States

Pump, Infusion, Implanted, Programmable

PMA: P800036 · Supplement: S038 · Decision Aug 1, 2014
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
S038
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
August 1, 2014
Date Received
June 27, 2014
Supplement Type
Normal 180 Day Track No User Fee
Supplement Reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR AN ALTERNATE STERILIZATION SITE LOCATED AT STERIS-ISOMEDIX (STERIS) IN NORTHBOROUGH, 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