# K052817: Eureka Infusion Pump, Models Eureka-IP, Eureka-LF

- Pathway: 510(k) (Traditional)
- Applicant: Universal Medical Technologies
- Decided: Apr 17, 2006 after 195 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 K896546 (1990). 3 ancestors in all.
No later device cites it as a predicate yet.
0 of 4 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K896546: Homepump (Disp. Elastomeric Infusion Device), Block Medical, Inc. (1990) Summary page 1.
- K923875: Sidekick 50 Plus and Sidekick 100 Plus, I-Flow Corp. (1993) Summary page 1.
- K931458: Medipak Ambulatory Infusion Pump, Medication Delivery Devices, Inc. (1994) Summary page 1.

## Indications for use
Infusions Of volumes between 50 ml. to 100 ml, Via Intravenous catheter or central IV line or subcutaneous route In Ambulatory, Ilome or I lospital Setting For General Use

Source page: https://510kreport.com/device/K052817
Methodology: https://510kreport.com/methodology