SIEMENS INFINITY SC 6002XL MODIFICATIONS— 510(k) K020144
Substantially EquivalentSiemens Medical Solutions USA, Inc.
FDA 510(k) clearance K020144 for SIEMENS INFINITY SC 6002XL MODIFICATIONS, Substantially Equivalent on 2002-02-15. Applicant: Siemens Medical Solutions USA, Inc..
Clearance details
- Applicant
- Siemens Medical Solutions USA, Inc.
- Product code
- Code DRT
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Danvers, MA, US
Adverse events under product code DRT
product code DRT- Death
- 4
- Total
- 4
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.