# K933404: Critikon Central Statin Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Critikon Company, LLC
- Decided: Feb 9, 1994 after 212 days
- Product code: DPS (Electrocardiograph)
- Device class: 2
- Regulation: 21 CFR 870.2340
- 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; 2 cite 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
- K980045: Centurion Central Station Arrhythmia Patient Monitoring System (1998), 0 descendants of its own
- K972498: Observer * Central Station (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K933404
Methodology: https://510kreport.com/methodology