FDA PMA FDA Class 3 Approved 🇺🇸 United States

Automated Insulin Dosing Device System, Single Hormonal Control

PMA: P160017 · Supplement: S014 · Decision Jun 29, 2017
Classifications
1
FEI Numbers
16
Registration Numbers
16

Basic Information

Device Name
Automated Insulin Dosing Device System, Single Hormonal Control
Trade Name
MiniMed 670G System
PMA Number
P160017
Supplement Number
S014
Device Class
FDA Class 3
Product Code
OZP
Generic Name
Automated insulin dosing device system, single hormonal control
Medical Specialty
Unknown
Advisory Committee
Clinical Chemistry
Decision
Approved
Decision Code
APPR
Decision Date
June 29, 2017
Date Received
June 2, 2017
Supplement Type
Special (Immediate Track)
Supplement Reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Expedited Review
N

Advisory Committee Statement

Approval for a test method change for the keypad assembly used in the MiniMed 630G and 670G Insulin Pumps.

Classifications

This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.

Product Code Device Name
OZP Automated Insulin Dosing Device System, Single Hormonal Control