# K221764: InBody Blood pressure monitor, Model BPBIO480KV

- Pathway: 510(k) (Traditional)
- Applicant: Inbody Co., Ltd.
- Decided: Oct 7, 2022 after 112 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: 3 generations back to K010828 (2001). 3 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 5 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K200442: InBody, Inbody Co., Ltd. (2020) Summary page 4.

## Most influential descendants
- K250091: KOROT Blood Pressure Monitor (KOROT P3 Accurate) (2025), 0 descendants of its own

## Indications for use
This blood pressure monitor is designed to measure blood pressure (diastolic and systolic) and pulse rate in adult patients with arm circumference range between 22 cm - 42 cm.

Source page: https://510kreport.com/device/K221764
Methodology: https://510kreport.com/methodology