Arm Blood Pressure Monitor (MJ1L, MJ2L, RN3L, RN4L,RN5L)— 510(k) K251143

Substantially Equivalent

Ningbo Ranor Medical Science & Technology Co., Ltd.

FDA 510(k) clearance K251143 for Arm Blood Pressure Monitor (MJ1L, MJ2L, RN3L, RN4L,RN5L), Substantially Equivalent on 2025-12-19. Applicant: Ningbo Ranor Medical Science & Technology Co., Ltd..

Clearance details

Applicant: Ningbo Ranor Medical Science & Technology Co., Ltd.
Product code: Code DXN
Advisory panel: Cardiovascular
Date received: 2025-04-14
Decision date: 2025-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ningbo, CN

Download summary PDF View on FDA.gov ↗

Adverse events under product code DXN

product code DXN

Death: 3
Injury: 169
Malfunction: 1,019
Other: 2
Total: 1,193

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.