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Index/Esaote Europe B.V.
ALT-001886K061755Amber Status

Esaote Europe B.V.

MYLAB15/20 NEW INDICATIONS ULTRASOUND SYSTEM

All identifiers (2)
Aletia (canonical)ALT-001886
FDA 510(k) ยท US (primary)K061755

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K061755
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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