# K003611: Pain Care Multi-Port Catheter, Model 2000L

- Pathway: 510(k) (Special)
- Applicant: Breg, Inc.
- Decided: Dec 13, 2000 after 21 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
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K031600: Conduction Catheter (2003), 1 descendant of its own
- K060119: Mckinley Saturation Catheter (2006), 0 descendants of its own

Source page: https://510kreport.com/device/K003611
Methodology: https://510kreport.com/methodology