# K192807: Duo-Flow Side x Side Double Lumen Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Medical Components, Inc. (dba MedComp)
- Decided: Apr 23, 2020 after 205 days
- Product code: MPB (Catheter, Hemodialysis, Non-Implanted)
- Device class: 2
- Regulation: 21 CFR 876.5540
- 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 K955002 (1996). 1 ancestor in all.
1 later device descends 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)
- K955002: Mahurkar 8 FR Dual Lemen Catheter, Quinton, Inc. (1996) Summary page 4.

## Most influential descendants
- K250836: 14F Duo-Flow® Side X Side Double Lumen Catheter (2025), 0 descendants of its own

## Indications for use
The Duo-Flow Side x Side Double Lumen Catheter is intended for short-term central venous access for hemodialysis, apheresis, and infusion.

Source page: https://510kreport.com/device/K192807
Methodology: https://510kreport.com/methodology