# K002739: Infusor Patient Control Module, 2ML, Model 2C1067K

- Pathway: 510(k) (Special)
- Applicant: Baxter Healthcare Corp
- Decided: Sep 11, 2000 after 10 days
- Product code: MEA (Pump, Infusion, Pca)
- 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
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have 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
- K051253: Modification to: Multirate Infusor SV )with and Without PCM), Multirate Infusor LV (with and Without PCM) (2005), 2 descendants of its own
- K131247: Multibolus II Disposable Pain Management System (2013), 0 descendants of its own
- K060933: Solace Post-Operative Pain Relief Infusion System (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K002739
Methodology: https://510kreport.com/methodology