FDA PMA FDA Class 3 Approved 🇺🇸 United States

Automated Insulin Dosing Device System, Single Hormonal Control

PMA: P160017 · Supplement: S095 · Decision Dec 17, 2021
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
S095
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
December 17, 2021
Date Received
November 17, 2021
Supplement Type
Special (Immediate Track)
Supplement Reason
Labeling Change - Indications/instructions/shelf life/tradename
Expedited Review
N

Advisory Committee Statement

Approval for approval for a labeling update to provide additional clarity on an existing warning for acetaminophen interference to the continuous glucose monitoring (CGM) component of the system.

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