FDA PMA FDA Class 3 Approved 🇺🇸 United States

Sensor, Glucose, Invasive

PMA: P980022 · Supplement: S107 · Decision Feb 6, 2012
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
CARELINK IPRO THERAPY MANAGEMENT SOFTWARE (MODEL, MMT-7340)
PMA Number
P980022
Supplement Number
S107
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
February 6, 2012
Date Received
December 12, 2011
Supplement Type
Real-Time Process
Supplement Reason
Change Design/Components/Specifications/Material
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR SOFTWARE CHANGES TO THE CARELINK IPRO THERAPY MANAGEMENT SOFTWARE (MMT-7340, VERSION 1.4A) FOR USE WITH THE DEVICE.

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