Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V3.1— 510(k) K182679
Substantially EquivalentCanon Medical Systems Corporation
FDA 510(k) clearance K182679 for Aplio i900/i800/i700/i600 Diagnostic Ultrasound System, V3.1, Substantially Equivalent on 2018-10-31. Applicant: Canon Medical Systems Corporation.
Clearance details
- Applicant
- Canon Medical Systems Corporation
- Product code
- Code IYN
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Otawara-Shi, JP
Adverse events under product code IYN
product code IYN- Death
- 25
- Injury
- 163
- Malfunction
- 1,538
- Other
- 4
- Total
- 1,730
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.