DINIMAP MODEL 827A— 510(k) K771782
Substantially EquivalentApplied Medical Research
FDA 510(k) clearance K771782 for DINIMAP MODEL 827A, Substantially Equivalent on 1977-10-04. Applicant: Applied Medical Research.
Clearance details
- Applicant
- Applied Medical Research
- Product code
- Code DXN
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Mchenry, IL, 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.