Digital Blood Pressure Monitor (Arm Type)— 510(k) K231245
Substantially EquivalentGuangdong Genial Technology Co., Ltd.
FDA 510(k) clearance K231245 for Digital Blood Pressure Monitor (Arm Type), Substantially Equivalent on 2023-11-22. Applicant: Guangdong Genial Technology Co., Ltd..
Clearance details
- Applicant
- Guangdong Genial Technology Co., Ltd.
- Product code
- Code DXN
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Zhaoqing, CN
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, through . 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.