FDA PMA FDA Class 3 30-Day Notice Accepted 🇺🇸 United States

Automated Insulin Dosing , Threshold Suspend

PMA: P120010 · Supplement: S116 · Decision May 30, 2018
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Automated Insulin Dosing , Threshold Suspend
Trade Name
MiniMed 530G Insulin Pump
PMA Number
P120010
Supplement Number
S116
Device Class
FDA Class 3
Product Code
OZO
Generic Name
Automated insulin dosing , threshold suspend
Medical Specialty
Unknown
Advisory Committee
Clinical Chemistry
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
May 30, 2018
Date Received
April 30, 2018
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Change from a manual to an automated pull test system to decrease variability and increase production capacity for the Paradigm and 530G insulin pumps housing. The Paradigm insulin pumps are components of the Continuous Glucose Monitoring System, Paradigm REAL-Time Revel System, and Paradigm REAL-Time System and the MiniMed 530G pumps are components of the MiniMed 530G System.

Classifications

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

Product Code Device Name
OZO Automated Insulin Dosing , Threshold Suspend