Class Class II

Aplio beyond and Aplio me Software V2.0 Diagnostic Ultrasound System (K253597)

K253597 2026-01-20 Traditional
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Description

Aplio beyond and Aplio me Software V2.0 Diagnostic Ultrasound System by Canon Medical Systems Corporation, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253597
Clearance Date2026-01-20
Clearance TypeTraditional
Product CodeIYN
Regulation Number892.1550

Categories

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