# K001317: ARIA

- Pathway: 510(k) (Abbreviated)
- Applicant: Del Mar Medical Systems, LLC
- Decided: Jul 21, 2000 after 86 days
- Product code: MWJ (Electrocardiograph, Ambulatory (Without Analysis))
- Device class: 2
- Regulation: 21 CFR 870.2800
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
25 later devices descend from it; 1 cites it directly.
0 of 26 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
- K021470: Seer Light Compact Digital Holter Recorder (2002), 24 descendants of its own
- K073545: Audicor, Hemo Ambulatory Monitor (2008), 11 descendants of its own
- K050731: Seer Light Extend Compact Digital Holter System (2005), 10 descendants of its own
- K112921: Medicalgorithmics Unified Arrhythmia Diagnostic System (2012), 7 descendants of its own
- K124060: Medical Gorithmics Unified Arrhythmia Diagnostic System (2013), 5 descendants of its own

Source page: https://510kreport.com/device/K001317
Methodology: https://510kreport.com/methodology