# K131103: Xres Blood Collection Reservoir Xres 120MICROMETER Blood Collection Reservoir

- Pathway: 510(k) (Special)
- Applicant: Sorin Group Italia S.R.L.
- Decided: Jun 6, 2013 after 48 days
- Product code: DTN (Reservoir, Blood, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4400
- 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 K100507 (2010). 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)
- K100507: Xres Blood Collection Reservoir, Sorin Group Italia S.R.L. (2010) Summary page 1.

## Most influential descendants
- K241236: XTRA Collection sets; XTRA Sequestration set X (2024), 0 descendants of its own

## Indications for use
The device is an accessory to an autotransfusion device and is intended for the sterile collection and filtration of recovered blood for subsequent processing for autotransfusion The device is an accessory to an autotransfusion device and is intended for the sterile collection and filtration of recovered blood for subsequent processing for autotransfusion

Source page: https://510kreport.com/device/K131103
Methodology: https://510kreport.com/methodology