# K092806: Auto Digital Upper Arm Blood Pressure Monitor, Model KP-7770

- Pathway: 510(k) (Special)
- Applicant: K-Jump Health Co., Ltd.
- Decided: Oct 9, 2009 after 28 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
Longest line of descent: 1 generation back to K083753 (2009). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K083753: Smart-Logic Auto Digital Upperarm Blood Pressure Monitor, Model KP-7500, Fully Fuzzy Auto Digital Upper Arm Blood Pressu, K-Jump Health Co., Ltd. (2009) Summary page 1.

## Indications for use
The KP-7770 is intended to measure the systolic and diastolic blood pressure and pulse rate (heart rate) by using an inflating cuff wrapped around the arm. It is indicated for use in adults. The devices display irregular pulse detection (IPD) icon on LCD screen when irregular pulse is detected during blood pressure measurement.

Source page: https://510kreport.com/device/K092806
Methodology: https://510kreport.com/methodology