# K200287: BP-BT Kiosk

- Pathway: 510(k) (Traditional)
- Applicant: Ld Technology, LLC
- Decided: May 15, 2020 after 100 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: 4 generations back to K982481 (1998). 6 ancestors in all.
No later device cites it as a predicate yet.
0 of 7 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K151953: A&D Medical TM-2657 Family of Digital Blood Pressure Monitors, A&D Company, Ltd. (2016) Summary page 4.

## Indications for use
BP-BT Kiosk is designed to measure blood pressure (systolic and diastolic) and pulse rate in adult patients with arm circumference range between 6.7 inches (17.0 cm) to 16.5 inches (42.0 cm). Indication: Prescription use in medical or clinic environment only.Rx only.

Source page: https://510kreport.com/device/K200287
Methodology: https://510kreport.com/methodology