FDA PMA FDA Class 3 Approved 🇺🇸 United States

Sensor, Glucose, Invasive

PMA: P980022 · Supplement: S090 · Decision Jan 7, 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
S090
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 7, 2011
Date Received
November 8, 2010
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A MODIFICATION TO THE DESIGN SPECIFICATION OF THE LUMEN TUBING USED IN THE MANUFACTURING PROCESS OF THE GLUCOSE SENSOR TO ALLOW FOR LESS DIMENSIONAL VARIATION IN THE TUBING SUPPLIED BY THE TUBING VENDOR.

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