MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE— 510(k) K965068
Substantially EquivalentToshiba America Medical Systems, In.C
FDA 510(k) clearance K965068 for MAGNETIC RESONANC DVCE VISART V 3.5 SOFTWARE, Substantially Equivalent on 1997-07-15. Applicant: Toshiba America Medical Systems, In.C.
Clearance details
- Applicant
- Toshiba America Medical Systems, In.C
- Product code
- Code LNH
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
Adverse events under product code LNH
product code LNH- Death
- 11
- Injury
- 670
- Malfunction
- 1,460
- Other
- 2
- Total
- 2,143
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.