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

Sensor, Glucose, Invasive

PMA: P160007 · Supplement: S002 · Decision Apr 20, 2018
Classifications
1
FEI Numbers
23
Registration Numbers
23

Basic Information

Device Name
Sensor, Glucose, Invasive
Trade Name
Guardian Connect System
PMA Number
P160007
Supplement Number
S002
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
April 20, 2018
Date Received
March 29, 2018
Supplement Type
30-Day Notice
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Additional laser cutting equipment for manufacture of the Guardian Sensor (3). The Guardian Sensor (3) is a component of the MiniMed 630G System with SmartGuard, the Guardian Connect System, and the MiniMed 670G 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