FDA device listing

MMT-1760 MiniMed 670G Insulin Pump Kit,MMT-1780 MiniMed 670G Insulin Pump,MMT-1880 MiniMed 770G Insulin Pump,MMT-1884L…

FDA device listing 1929078790 · Medtronic

Key facts

Proprietary names MMT-1760 MiniMed 670G Insulin Pump Kit,MMT-1780 MiniMed 670G Insulin Pump,MMT-1880 MiniMed 770G Insulin Pump,MMT-1884L MiniMed 780G Insulin Pump,MMT-1884 MiniMed 780G Insulin Pump,MMT-1890 MiniMed 770G Insulin Pump Kit MG/DL,MMT-1894 MiniMed 780G Insulin Pump Kit,MMT-5120 Simplera Sync sensor,MMT-7020 Enlite 3 Sensor 5pk,MMT-7040 Guardian Sensor 4,MMT-7512 One-press Serter,MMT-7715 Charger…
Owner/operator Medtronic
Owner/operator number 10094334
Premarket submissions P160017
Product codes OZP
Device names OZP - Automated Insulin Dosing Device System, Single Hormonal Control
Device class Class III
Classification regulations (21 CFR) ORCA1.OZP
Review panels Clinical Chemistry
Registered establishments MEDTRONIC MINIMED, MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS
Establishment registrations 2032227, 3042027705
FEI numbers 3003166194, 3042027705
Establishment operations Complaint File Establishment, Manufacturer, Repackager/Relabeler
Registration valid through 2026

At a glance

  • 1–9 Registered establishments listing this device
  • 100–999 UDI devices (GUDID) under the same submission
  • 1–9 Device listings citing the same submission
  • Yes Premarket submission listed

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA device listings

Establishments that make or process devices for the U.S. market must list each device with the FDA. A listing records the device's proprietary names, product codes and premarket submission, and every registered establishment that handles it.

Source: U.S. Food and Drug Administration (FDA), Establishment Registration and Device Listing database

Browse all FDA device listings