# K952879: Sarns Centrifugal Pump with Duraflo II Treatment

- Pathway: 510(k) (Traditional)
- Applicant: Baxter Healthcare Corp
- Decided: Apr 22, 1996 after 304 days
- Product code: KFM (Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type)
- Device class: 2
- Regulation: 21 CFR 870.4360
- 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 K915363 (1993). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K915363: Sarns 7850 Centrifugal Pump (Modified), 3M Health Care, Ltd. (1993) Summary page 2.

## Indications for use
The 3M™ Sarns™ Centrifugal Pumps with Duraflo® [l Treatment are indicated as extracorporeal pumps for use in cardiopulmonary bypass procedures only and for use exclusively with Sarns™ centrifugal control systems.

Source page: https://510kreport.com/device/K952879
Methodology: https://510kreport.com/methodology