# K024084: Abbott Plum a+ Infusion Pump, Model 12391

- Pathway: 510(k) (Special)
- Applicant: Abbott Laboratories
- Decided: Dec 31, 2002 after 20 days
- Product code: FRN (Pump, Infusion)
- 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
No predicates in its family tree.
34 later devices descend from it; 4 cite it directly.
13 of 35 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) Abbott Plum A+ Infusion Pump: named in the summary without a submission number

## Most influential descendants
- K031185: Abbott Plum a+ Infusion Pump with a HPL/RS Plug-and-Play Module (2003), 32 descendants of its own
- K042081: Plum a+ Infusion System with Hospira Mednet Software , and Plum a+3 Infusion System with Hospira Mednet Software (2004), 27 descendants of its own
- K041550: Hospira Phoenix Infusion System with Hospira Mednet Software (2004), 13 descendants of its own
- K052052: Hospira Plum a+ Infusion Pump System V11.5, Hospira Plum a+ 3 Infusion Pump System, V11.5 (2005), 12 descendants of its own
- K103224: Hospira Plum Infusion Set; Hospira Infusion Set with Yellow Stripe Tubing (2011), 10 descendants of its own

## Indications for use
Indicated for use in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.

Source page: https://510kreport.com/device/K024084
Methodology: https://510kreport.com/methodology