# K955152: Stockert S3 Ups, LVL CTRL Bubb. Det., Dual Press. CTRL., Temp Mont., Timer

- Pathway: 510(k) (Traditional)
- Applicant: Stoeckert Instrumente
- Decided: Feb 22, 1996 after 101 days
- Product code: DTW (Monitor And/Or Control, Level Sensing, Cardiopulmonary Bypass)
- Device class: 2
- Regulation: 21 CFR 870.4340
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend 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)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K041558: Stockertir Purge Control (Apc) System (2004), 1 descendant of its own
- K103469: Stockert Air Purge Control System Model 23-45-05 (2011), 0 descendants of its own

Source page: https://510kreport.com/device/K955152
Methodology: https://510kreport.com/methodology