ALT-001913K062677Amber Status
Mortara Instrument, Inc.
ELI 350 ELECTROCARDIOGRAPH
All identifiers (2)
Aletia (canonical)
ALT-001913FDA 510(k) · US (primary)
K062677Regulatory Registrations
🌐
US
FDA
ID: K062677
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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