# K002074: AB Cardiette Daedalus View Base and AB Cardiettte Daedalus View Hes

- Pathway: 510(k) (Traditional)
- Applicant: H&C Medical Devices Spa
- Decided: Oct 4, 2000 after 86 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.
27 later devices descend from it; 4 cite it directly.
1 of 28 devices in its family (counting itself) has 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
- K051534: Cardioline AR 600, AR 1200, AR 2100 (2005), 17 descendants of its own
- K082124: Carditte Microtel (2009), 12 descendants of its own
- K070614: Corscreen (2007), 12 descendants of its own
- K080734: Flowscreen, Flowscreen/Corscreen, Flowscreen CT (2008), 10 descendants of its own
- K082539: Masterscope, Masterscope Ecg, Masterscope CT (2008), 9 descendants of its own

Source page: https://510kreport.com/device/K002074
Methodology: https://510kreport.com/methodology