# K052973: Ipump Pain Management System, Model 2L3107, 2L3107K

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Jan 25, 2007 after 458 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: 2 generations back to K926385 (1994). 2 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K993387: Ipump Pain Management System, Model 2L3107K, Baxter Healthcare Corp (1999) Summary page 1.

## Most influential descendants
- K120209: Patient Controlled Analgesia (Pca) Button Cable (2012), 1 descendant of its own
- K220695: Elite Biomedical Solutions Dose Request Cord (2022), 0 descendants of its own

## Indications for use
The Ipump TM Pain Management system is indicated for the controlled delivery (continuous, intermittent, and continuous plus intermittent) of analgesic, sedative, and anesthetic solutions through clinically acceptable routes of administration including intravenous, subcutaneous, and epidural, and for regional (local) analgesia applications.

Source page: https://510kreport.com/device/K052973
Methodology: https://510kreport.com/methodology