# K890282: Resubmitted Abbott Lifecare Model 3 HB Pump

- Pathway: 510(k) (Traditional)
- Applicant: Abbott Laboratories
- Decided: Apr 19, 1989 after 90 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.
1 of 2 devices in its family (counting itself) has 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
- K081412: Plum a+ Hyperbaric Infusion System with Hospira Mednet Software (2008), 0 descendants of its own

## Recalls of this device
- Nov 24, 2009 · Not classified · Z-1364-2010: Reports of difficulty in adjusting the flow rate, which could result in flow rate variances.

Source page: https://510kreport.com/device/K890282
Methodology: https://510kreport.com/methodology