Endocardial Solutions, Inc.

MODIFICATION TO ENSITE 3000 SYSTEM, MODEL EE3000

All identifiers (2)

Aletia (canonical)ALT-001517

FDA 510(k) · US (primary)K030129

Regulatory Registrations

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FDA

ID: K030129

510k

Last Automated Sync

Mar 2026

Last Clinical Review

Not reviewed

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