# K992599: Dideco Ats Autotransfusion Cardiotomy Reservoir

- Pathway: 510(k) (Abbreviated)
- Applicant: Dideco S.P.A.
- Decided: Nov 1, 1999 after 90 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 K884872 (1989). 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)
- K884872: Dideco-Shiley Autotransfusion Cardiotomy Reservoir, Shiley, Inc. (1989) Summary page 1.

## Indications for use
The Dideco ATS Autotransfusion Cardiotomy Reservoir 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/K992599
Methodology: https://510kreport.com/methodology