# K083753: Smart-Logic Auto Digital Upperarm Blood Pressure Monitor, Model KP-7500, Fully Fuzzy Auto Digital Upper Arm Blood Pressu

- Pathway: 510(k) (Abbreviated)
- Applicant: K-Jump Health Co., Ltd.
- Decided: Jun 19, 2009 after 184 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.
1 later device descends from it; 1 cites it directly.
0 of 2 devices 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-6210: named in the summary without a submission number
- (no number) K-jump Health Co., Ltd.'s Arm BPM Blood Pressure Monitor Model KP-6821 and KP-6822: named in the summary without a submission number
- (no number) MicroLife's Upper Arm Blood Pressure Monitor Model BP-3BTO-AP: named in the summary without a submission number

## Most influential descendants
- K092806: Auto Digital Upper Arm Blood Pressure Monitor, Model KP-7770 (2009), 0 descendants of its own

## Indications for use
The KP-7500 and KP-7500D are intended to measure the systolic and diastolic blood pressure and pulse rate (heart rate) by using an inflating cuff which is 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/K083753
Methodology: https://510kreport.com/methodology