Ultimax-i, DREX-UI80 (V1.60)— 510(k) K181834
Substantially EquivalentCanon Medical Systems Corporation
FDA 510(k) clearance K181834 for Ultimax-i, DREX-UI80 (V1.60), Substantially Equivalent on 2018-07-19. Applicant: Canon Medical Systems Corporation.
Clearance details
- Applicant
- Canon Medical Systems Corporation
- Product code
- Code OWB
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Otawara-Shi, JP
Adverse events under product code OWB
product code OWB- Death
- 49
- Injury
- 340
- Malfunction
- 36,973
- Total
- 37,362
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.