# K123600: Digital Blood Pressure Monitor

- Pathway: 510(k) (Traditional)
- Applicant: Little Doctor Electronic (Nantong)Co.,Ltd
- Decided: May 3, 2013 after 163 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 no predicate by number.

## Indications for use
The Electronic Blood Pressure Monitor LD-568, LO-520, LD-522, LD-587 & LD-528 is device intended to measure the systolic and diastolic blood pressure and pulse rate of an adult individual by using a non-invasive technique in which an inflatable cuff is wrapped around the arnm.

Source page: https://510kreport.com/device/K123600
Methodology: https://510kreport.com/methodology