# K933960: Plasma Recovery Program for the Cobe Brat 2 Autologous Blood Salvage System

- Pathway: 510(k) (Traditional)
- Applicant: Cobe Cardiovascular, Inc.
- Decided: Jun 10, 1994 after 298 days
- Product code: CAC (Apparatus, Autotransfusion)
- Device class: 2
- Regulation: 21 CFR 868.5830
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
3 later devices descend from it; 1 cites it directly.
0 of 4 devices in its family (counting itself) have a Class I recall.

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

## Most influential descendants
- K962689: Cobe Brat 2 Autologous Blood Salvage System with Modified Plasma Recovery Program (PRP) (1997), 2 descendants of its own
- K974897: Cobe Brat 2 System with Modified Standard Volume Processing Set (1998), 0 descendants of its own
- K973627: Standard Volume Processing Set for the Cobe Brat 2 Autologous Blood Salvage System (1997), 0 descendants of its own

Source page: https://510kreport.com/device/K933960
Methodology: https://510kreport.com/methodology