ELECTRONIC BLOOD PRESS. METER-ZH-820P— 510(k) K832075
Substantially EquivalentPanasonic Co. Div. Matsu Elec. Corp. America
FDA 510(k) clearance K832075 for ELECTRONIC BLOOD PRESS. METER-ZH-820P, Substantially Equivalent on 1983-08-12. Applicant: Panasonic Co. Div. Matsu Elec. Corp. America.
Clearance details
- Applicant
- Panasonic Co. Div. Matsu Elec. Corp. America
- Product code
- Code DXN
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Nutley, NJ, 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.