Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V8.5— 510(k) K242808

Substantially Equivalent

Canon Medical Systems Corporation

FDA 510(k) clearance K242808 for Aplio i900/i800/i700 Diagnostic Ultrasound System, Software V8.5, Substantially Equivalent on 2025-05-13. Applicant: Canon Medical Systems Corporation. Device class: 2.

Clearance details

Applicant
Canon Medical Systems Corporation
Product code
Code IYN
Device class
Class 2
Regulation
21 CFR 892.1550
Advisory panel
Radiology
Date received
Decision date
Decision
Substantially Equivalent
Clearance type
Traditional
Location
Otawara-Shi, JP
Download summary PDFView on FDA.gov ↗

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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.