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

Automated Insulin Dosing , Threshold Suspend

PMA: P120010 · Supplement: S027 · Decision Jul 24, 2014
Classifications
1
FEI Numbers
18
Registration Numbers
18

Basic Information

Device Name
Automated Insulin Dosing , Threshold Suspend
Trade Name
ENLITE GLUCOSE SENSOR
PMA Number
P120010
Supplement Number
S027
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
July 24, 2014
Date Received
June 23, 2014
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

CHANGE IN THE CONCENTRATION OF A RAW MATERIAL USED DURING MANUFACTURE OF THE ENLITETM GLUCOSE SENSOR (MMT-7008) OF THE MINIMED 530G SYSTEM AND SOFTM GLUCOSE SENSOR (MMT-7002, MMT-7003) OF THE PARADIGM® REAL-TIME SYSTEM AND PARADIGM® REAL-TIME REVEL 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