SYNAPSE 3D LUNG AND ABDOMEN ANALYSIS— 510(k) K130542
Substantially EquivalentFujifilm Medical System U.S.A., Inc.
FDA 510(k) clearance K130542 for SYNAPSE 3D LUNG AND ABDOMEN ANALYSIS, Substantially Equivalent on 2013-06-14. Applicant: Fujifilm Medical System U.S.A., Inc..
Clearance details
- Applicant
- Fujifilm Medical System U.S.A., Inc.
- Product code
- Code LLZ
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Stamford, CT, US
Adverse events under product code LLZ
product code LLZ- Death
- 13
- Total
- 13
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.