Class Class II

Aplio i900, Aplio i800 and Aplio i700 Software V9.0 Diagnostic Ultrasound System (K252074)

K252074 2025-10-31 Traditional
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Description

Aplio i900, Aplio i800 and Aplio i700 Software V9.0 Diagnostic Ultrasound System by Canon Medical Systems Corporation, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252074
Clearance Date2025-10-31
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

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