# K022916: Blood Pressure Monitor Smartlogic, Models KP-6210 and KP-6211

- Pathway: 510(k) (Special)
- Applicant: K-Jump Health Co., Ltd.
- Decided: Nov 21, 2002 after 79 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) Wristwatch BPM model KP-6120: named in the summary without a submission number
- (no number) SmartInflate CardioPro model 1000i: named in the summary without a submission number
- (no number) SmartInflate CardioPro model 3000i: named in the summary without a submission number

## Indications for use
The Blood Pressure Monitor Smartlogic models KP-6210 and KP-6211 are intended to measure the blood pressure of the systolic, diastolic, and pulse rate by using an inflating cuff. The devices are indicated for use in adults.

Source page: https://510kreport.com/device/K022916
Methodology: https://510kreport.com/methodology