# K952660: Braun Hemodialysis Catheter

- Pathway: 510(k) (Traditional)
- Applicant: B.Braun Medical, Inc.
- Decided: Sep 17, 1996 after 463 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 K893439 (1989). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K893439: Hemo-Cath Silicone Double Lumen Cath SL28C & SL40C, Medical Components, Inc. (1989) Summary page 1.
- K941851: Dual Lumen Catheter (DLC) Tray, Neostar Medical Technologies, Inc. (1995) Summary page 1.

## Indications for use
The intended use is to allow access to the central venous system for blood circulation in pheresis or apheresis processes(i.e. Hemodialysis).

Source page: https://510kreport.com/device/K952660
Methodology: https://510kreport.com/methodology