# K001828: Paradigm 1.5ML Reservoir, Model 326

- Pathway: 510(k) (Traditional)
- Applicant: Minimed, Inc.
- Decided: Aug 18, 2000 after 63 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- 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

Source page: https://510kreport.com/device/K001828
Methodology: https://510kreport.com/methodology