# K935732: Cardio Perfect ST 2001

- Pathway: 510(k) (Traditional)
- Applicant: Cardio Control BV
- Decided: Apr 4, 1996 after 855 days
- Product code: DSI (Detector And Alarm, Arrhythmia)
- Device class: 2
- Regulation: 21 CFR 870.1025
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
11 later devices descend from it; 1 cites it directly.
0 of 12 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names no predicate by number.

## Most influential descendants
- K052158: Welch Allyn Cardioperfect Workstation Version 1.5.0 Software (2005), 10 descendants of its own
- K082478: Welch Allyn Cardioperfect Workstation Software (CPWS)  V 1.62 (2009), 4 descendants of its own
- K141546: Vitalograph Model 7000 Spirotrac (2014), 2 descendants of its own
- K090602: Cardiodynamics Bioz RX, Model 7101-Sys (2009), 1 descendant of its own
- K201562: Spirotrac (2020), 0 descendants of its own

Source page: https://510kreport.com/device/K935732
Methodology: https://510kreport.com/methodology