# K170151: Electronic Blood Pressure Monitor

- Pathway: 510(k) (Special)
- Applicant: Shenzhen Pango Electronic Co., Ltd.
- Decided: Oct 13, 2017 after 269 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: 5 generations back to K001670 (2000). 5 ancestors in all.
19 later devices descend from it; 5 cite it directly.
0 of 25 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K131558: PG-800B Series, Including PG-800BD, PG-800B-1, PG-800BD-1, PG-800B3, PG-800B4, PG-800B4D, PG-800B5, PG-800B5-1, PG-800B6, Shenzhen Pango Electronic Co., Ltd. (2013) Summary page 6.

## Most influential descendants
- K182495: Electronic Blood Pressure Monitor (2019), 11 descendants of its own
- K191180: Electronic Blood Pressure Monitor (2019), 10 descendants of its own
- K222125: Arm Blood Pressure Monitor, models AOJ-30A, AOJ-30B, AOJ-30C, AOJ-30D, AOJ-30E, AOJ-30F and AOJ-30G (2022), 4 descendants of its own
- K183058: Arm-type Electronic Blood Pressure Monitor (2019), 3 descendants of its own
- K222994: Arm Blood Pressure Monitor, models AOJ-33A and AOJ-33B (2023), 1 descendant of its own

## Indications for use
The Electronic Blood Pressure Monitor is intended to measure the systolic and diastolic blood pressure as well as the pulse rate of adult person via non-invasive oscillometric technique in which an inflatable cuff is wrapped around the upper arm. It can be used at medical facilities or at home. The intended arm circumference includes 22 cm~32 cm and 32 cm~42 cm.

Source page: https://510kreport.com/device/K170151
Methodology: https://510kreport.com/methodology