FDA PMA FDA Class 3 Approved 🇺🇸 United States

Sensor, Glucose, Invasive

PMA: P980022 · Supplement: S092 · Decision Jan 31, 2011
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
MEDTRONIC MINIMED CONTINUOUS GLUCOSE MONITORING SYSTEM
PMA Number
P980022
Supplement Number
S092
Device Class
FDA Class 3
Product Code
MDS
Generic Name
Sensor, glucose, invasive
Medical Specialty
Unknown
Advisory Committee
Clinical Chemistry
Decision
Approved
Decision Code
APPR
Decision Date
January 31, 2011
Date Received
December 15, 2010
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A SOFTWARE CHANGE TO THE CARELINK PERSONAL THERAPY MANAGEMENT SOFTWARE FOR DIABETES, MMT-7333, FROM VERSION 5.3A TO 5.4A.

Classifications

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

Product Code Device Name
MDS Sensor, Glucose, Invasive