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

Sensor, Glucose, Invasive

PMA: P120005 · Supplement: S058 · Decision Jan 19, 2017
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM
PMA Number
P120005
Supplement Number
S058
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 19, 2017
Date Received
December 21, 2016
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Qualification of additional manufacturing space for the manufacture of the G5 Mobile Receiver. The G5 Mobile Receiver is a component of the G5 Mobile 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