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

Sensor, Glucose, Invasive

PMA: P050020 · Supplement: S015 · Decision Jun 24, 2009
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
FREESTYLE NAVIGATOR CONTINUOUS GLUCOSE MONITORING SYSTEM
PMA Number
P050020
Supplement Number
S015
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
June 24, 2009
Date Received
June 4, 2009
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

CHANGE TO THE MOLD TEMPERATURE.

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