INFX-8000V, INFINIX-CFI AND INFINIX VFI— 510(k) K081582
Substantially EquivalentToshiba America Medical Systems, In.C
FDA 510(k) clearance K081582 for INFX-8000V, INFINIX-CFI AND INFINIX VFI, Substantially Equivalent on 2008-06-17. Applicant: Toshiba America Medical Systems, In.C.
Clearance details
- Applicant
- Toshiba America Medical Systems, In.C
- Product code
- Code JAA
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Tustin, CA, US
Adverse events under product code JAA
product code JAA- Other
- 1
- Total
- 1
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.