# K120209: Patient Controlled Analgesia (Pca) Button Cable

- Pathway: 510(k) (Traditional)
- Applicant: American I.V. Products, Inc.
- Decided: Apr 12, 2012 after 79 days
- Product code: MRZ (Accessories, 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: 3 generations back to K926385 (1994). 4 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 6 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K052973: Ipump Pain Management System, Model 2L3107, 2L3107K, Baxter Healthcare Corp (2007) Summary page 3.
- K993387: Ipump Pain Management System, Model 2L3107K, Baxter Healthcare Corp (1999) Summary page 3.
- K022203: Abbott Lifecare Pca 3 Infuser, Model 12384, Abbott Laboratories (2002) Summary page 3.

## Most influential descendants
- K220695: Elite Biomedical Solutions Dose Request Cord (2022), 0 descendants of its own

## Indications for use
This device is an accessory for a syringe or infusion pump. The healthcare worker connects the device to the corresponding pump. The patient uses the switch on the cable to signal the syringe pump to deliver medication consistent with the parameters entered into the pump by the healthcare worker.

Source page: https://510kreport.com/device/K120209
Methodology: https://510kreport.com/methodology