Shenzhen Mindray Bio-Medical Electronics Co., Ltd.

MODIFICATION TO PM-8000 PATIENT MONITOR

All identifiers (2)

Aletia (canonical)ALT-001716

FDA 510(k) · US (primary)K043348

Regulatory Registrations

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FDA

ID: K043348

510k

Lifecycle Signals

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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