# K032005: Medtronic Minimed Paradigm Reservoir, Model MMT-332

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Minimed
- Decided: Aug 22, 2003 after 53 days
- Product code: FRN (Pump, Infusion)
- Device class: 2
- Regulation: 21 CFR 880.5725
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 2 cite it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Medtronic MiniMed Paradigm Reservoir Model MMT-326: named in the summary without a submission number

## Most influential descendants
- K210714: Extended Reservoir (2022), 1 descendant of its own
- K241622: Extended Reservoir; MiniMed Reservoir (2024), 0 descendants of its own

## Recalls of this device
- Jul 3, 2013 · Class II · Z-1986-2013: Medtronic is recalling certain lots of Medtronic MiniMed Paradigm Reservoirs MMT-326A (1.8mL) and MMT-332A (3.0mL) used with Medtronic Paradigm insulin pumps because they may have increased risk for l

## Indications for use
The Medtronic MiniMed Paradigm Reservoir MMT-332 is indicated for the subcutaneous infusion of medication, including insulin, from the Paradigm family of infusion pumps and infusion sets. The reservoir is not indicated for use with blood.

Source page: https://510kreport.com/device/K032005
Methodology: https://510kreport.com/methodology