# K003282: Full Auto Blood Pressure Monitor, Model SE-7700H

- Pathway: 510(k) (Traditional)
- Applicant: Sein Electronics Co., Ltd.
- Decided: Nov 1, 2000 after 13 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.
2 later devices descend from it; 1 cites 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 lists a 510(k) statement for it but has not posted the file, so its predicates are not known.

## Most influential descendants
- K032927: Full Auto Arm Digital Blood Pressure Monitor (2004), 1 descendant of its own
- K042014: Digital Blood Pressure Monitor, Models SE-9000, SE-9200 and SE-9400 (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K003282
Methodology: https://510kreport.com/methodology