# K913844: Accutracker DX

- Pathway: 510(k) (Traditional)
- Applicant: Suntech Medical Instruments, Inc.
- Decided: Jul 14, 1992 after 321 days
- Product code: DXN (System, Measurement, Blood-Pressure, Non-Invasive)
- Device class: 2
- Regulation: 21 CFR 870.1130
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
6 later devices descend from it; 3 cite it directly.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K031964: Bpcard (2003), 3 descendants of its own
- K073630: Modification to: Bpcard, Model Z-7000-0700 (2008), 2 descendants of its own
- K103703: Reguis Sigma (2011), 1 descendant of its own
- K120131: Regius SIGMA2 (2012), 0 descendants of its own
- K051368: BR 102 Plus Blood Pressure Holter System (2005), 0 descendants of its own

Source page: https://510kreport.com/device/K913844
Methodology: https://510kreport.com/methodology