Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

MODIFICATION TO: DP-9900 DIGITAL ULTRASONIC DIAGNOSTIC IMAGING SYSTEM, MODEL DP-9900

All identifiers (2)

Aletia (canonical)ALT-001838

FDA 510(k) · US (primary)K053346

Regulatory Registrations

🌐

FDA

ID: K053346

510k

Lifecycle Signals

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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