# K895429: A&D Automatic Digital Blood Pressure Meter 2650

- Pathway: 510(k) (Traditional)
- Applicant: A&D Engineering, Inc.
- Decided: Nov 28, 1989 after 84 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.
4 later devices descend from it; 2 cite it directly.
0 of 5 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
- K062462: Non-Invasive Blood Pressure Monitor, Models FT-500R/L and FT-700R/L (2006), 2 descendants of its own
- K092432: Automoatic Blood Pressure Monitor, Models: Easy X 800 and 900 (R/L) (2009), 1 descendant of its own
- K140762: Automatic Blood Pressure Monitor (2015), 0 descendants of its own
- K983855: Fuzzy Type Digital Blood Pressure Monitor, Model #'S HD-1000S & HD-2000F (1998), 0 descendants of its own

Source page: https://510kreport.com/device/K895429
Methodology: https://510kreport.com/methodology