Nihon Kohden America, Inc.

ECG-1250A SERIES CARDIOFAX S AND ECG-1350A SERIES CARDIOFAX M

All identifiers (2)

Aletia (canonical)ALT-001985

FDA 510(k) · US (primary)K072217

Regulatory Registrations

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FDA

ID: K072217

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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