# K952826: Full Auto Fuzzy Blood Pressure Meter Model SE-7000

- Pathway: 510(k) (Traditional)
- Applicant: Sein Electronics Co., Ltd.
- Decided: Nov 14, 1996 after 513 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.
3 later devices descend from it; 1 cites it directly.
0 of 4 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
- K992328: Fuzzy Automatic Blood Pressure Monitor Models MD-750, MD-770, MD-800 (1999), 2 descendants of its own
- K041491: Zewa MFM-007 Blood Pressure Monitor (2004), 0 descendants of its own
- K041789: Noninvasive Blood Pressure Monitor, Models MD-880B and MD-900T (2004), 0 descendants of its own

Source page: https://510kreport.com/device/K952826
Methodology: https://510kreport.com/methodology