# K040114: Abbott Data Port PC, Model 12181

- Pathway: 510(k) (Special)
- Applicant: Abbott Laboratories
- Decided: Jan 29, 2004 after 9 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
Longest line of descent: 1 generation back to K982159 (1999). 4 ancestors in all.
No later device cites it as a predicate yet.
1 of 5 devices in its family (counting itself) has a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K024084: Abbott Plum a+ Infusion Pump, Model 12391, Abbott Laboratories (2002) Summary page 3.
- K021350: Abbott Plum a+3 Multichannel Infusion Pump, Model 12348, Abbott Laboratories (2002) Summary page 3.
- K011442: Abbott Plum a+Infusion Pump, Model 11971, Abbott Laboratories (2001) Summary page 3.
- K982159: Abbott Plum a+ Infusion Pump, Abbott Laboratories (1999) Summary page 3.

## Indications for use
The device is used in parenteral, enteral and epidural therapies and the administration of whole blood and blood products.

Source page: https://510kreport.com/device/K040114
Methodology: https://510kreport.com/methodology