# K032492: Blood Pressure Monitor, Model KP-7000

- Pathway: 510(k) (Special)
- Applicant: K-Jump Health Co., Ltd.
- Decided: Sep 9, 2003 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
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) K-jump Health Co., Ltd.’s Wristwatch BPM Blood Pressure Monitor Model KP-6120: named in the summary without a submission number
- (no number) MicroLife’s Wrist Watch Blood Pressure Monitor Model BP-3BU1-3: named in the summary without a submission number

## Indications for use
The KP-7000 is intended to measure the systolic and diastolic blood pressure and pulse rate (heart rate) by using an inflating cuff which is wrapped around the wrist. It is indicated for use in adults.

Source page: https://510kreport.com/device/K032492
Methodology: https://510kreport.com/methodology