Ge Medical Systems Information Technologies

DINAMAP PRO SERIES MONITOR, MODELS 110, 210, 310, 410

All identifiers (2)

Aletia (canonical)ALT-001410

FDA 510(k) · US (primary)K020022

Regulatory Registrations

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FDA

ID: K020022

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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