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

Automated Insulin Dosing , Threshold Suspend

PMA: P120010 · Supplement: S006 · Decision Dec 5, 2013
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
S006
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
December 5, 2013
Date Received
November 8, 2013
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

PC-BASED MANUFACTURING SOFTWARE UPDATE FROM VERSION 2.2A TO VERSION 2.3A AT THE MEDTRONIC MINIMED, NORTHRIDGE FACILITY, AND UPDATE FROM VERSION 2.0D TO VERSION 2.3A AT THE MPROC, JUNCOS FACILITY FOR THE PARADIGM REAL-TIME INSULIN PUMP (MODELS: MMT-522, MMT-522K, MMT-722, AND MMT-722K), THE PARADIGM REAL-TIME REVEL INSULIN PUMP (MODELS: MMT-523, MMT-523K, MMT-723, AND MMT-723K), THE GUARDIAN REAL-TIME MONITOR (MODEL: CSS7100) AND THE MINIMED 530G INSULIN PUMP (MODELS MMT-551 AND MMT-751).

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