# K990259: Disetronic Multifuse Infusion Pump System

- Pathway: 510(k) (Special)
- Applicant: Disetronic Medical Systems
- Decided: Feb 12, 1999 after 16 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 K915566 (1992). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K915566: Disetronic Panomat Pump, Disetronic Medical Systems (1992) Summary page 1.

## Indications for use
The Disetronic Multifuse Infusion Pump, with its accessories, is indicated for the controlled delivery of parenteral fluids, including patient controlled analgesia (PCA), in both the hospital and home care environments.

Source page: https://510kreport.com/device/K990259
Methodology: https://510kreport.com/methodology