# K960001: Minimed Infusion Pump, Model MMT-507

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Minimed
- Decided: Apr 30, 1996 after 119 days
- Product code: LZG (Pump, Infusion, Insulin)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K901588 (1990). 1 ancestor in all.
13 later devices descend from it; 1 cites it directly.
1 of 15 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K901588: Minimed (R) Model 506 External Insulin Pump, Medtronic Minimed (1990) Summary page 1.

## Most influential descendants
- K013309: Glucopro Evo Infusion Pump (2002), 12 descendants of its own
- K050312: Amigo Insulin Pump (2005), 11 descendants of its own
- K071613: Amigo Insulin Pump (2007), 10 descendants of its own
- K111210: T:Slim (TM) Insulin Delivery System (2011), 9 descendants of its own
- K133593: T:Slim Insulin Delivery System (2014), 8 descendants of its own

## Indications for use
The MMT-507 is intended for continuous delivery of insulin, at set and variable rates, for the management of diabetes mellitus in persons requiring insulin.

Source page: https://510kreport.com/device/K960001
Methodology: https://510kreport.com/methodology