FDA PMA FDA Class 3 Approved 🇺🇸 United States

Sensor, Glucose, Invasive

PMA: P980022 · Supplement: S105 · Decision Apr 25, 2012
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
GUARDIAN REAL-TIME SYSTEM
PMA Number
P980022
Supplement Number
S105
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
April 25, 2012
Date Received
November 22, 2011
Supplement Type
135 Review Track For 30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

APPROVAL FOR A MANUFACTURING LOCATION CHANGE FROM CHINA TO VIETNAM.

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