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

Sensor, Glucose, Invasive

PMA: P120005 · Supplement: S032 · Decision Jan 22, 2015
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
DEXCOM G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM
PMA Number
P120005
Supplement Number
S032
Device Class
FDA Class 3
Product Code
MDS
Generic Name
Sensor, glucose, invasive
Medical Specialty
Unknown
Advisory Committee
Clinical Chemistry
Decision
30-Day Notice Accepted
Decision Code
OK30
Decision Date
January 22, 2015
Date Received
December 23, 2014
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

CHANGE TO THE MANUFACTURING OF THE SENSOR COMPONENT ADHESIVE PATCH TO SUPPORT PEEL ADHESION TEST SPECIFICATIONS. THE SENSOR IS A COMPONENT OF THE G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM.

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