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

Automated Insulin Dosing , Threshold Suspend

PMA: P120010 · Supplement: S051 · Decision Jan 14, 2015
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Automated Insulin Dosing , Threshold Suspend
Trade Name
MINI-MED 530G INSULIN PUMP
PMA Number
P120010
Supplement Number
S051
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
January 14, 2015
Date Received
December 15, 2014
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

A CHANGE IN TERTIARY SUPPLIERS AND METHOD FOR THE NICKEL AND GOLD PLATING PROCESS FOR THE KEYPAD FLEXIBLE CIRCUIT FOR THE PARADIGM REAL-TIME INSULIN PUMP (MMT-522, MMT-522K, MMT-722, MMT-722K), PARADIGM REAL-TIME REVEL INSULIN PUMP (MMT-523,MMT-523K, MMT-723, MMT-723K) AND MINIMED 530G INSULIN PUMP (MMT-551, MMT-751) THAT ARE PART OF THE PARADIGM REAL-TIME SYSTEM, THE PARADIGM REAL-TIME REVEL SYSTEM AND THE MINIMED 530G SYSTEM, RESPECTIVELY.

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