MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR— 510(k) K003444
Substantially EquivalentNihon Seimitsu Sokki Co., Ltd.
FDA 510(k) clearance K003444 for MODEL WS-500 DIGITAL WRIST BLOOD PRESSURE MONITOR, Substantially Equivalent on 2000-11-21. Applicant: Nihon Seimitsu Sokki Co., Ltd..
Clearance details
- Applicant
- Nihon Seimitsu Sokki Co., Ltd.
- Product code
- Code DXN
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Smithfield, VA, US
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.