ALT-001422K020494Amber Status
Philips Medical Systems, Inc.
MODIFICATION TO M2376A DEVICELINK SYSTEM
All identifiers (2)
Aletia (canonical)
ALT-001422FDA 510(k) · US (primary)
K020494Regulatory Registrations
🌐
US
FDA
ID: K020494
510k
Lifecycle Signals
Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
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