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Index/Elekta Instrument AB
ALT-001553K031999Amber Status

Elekta Instrument AB

ELEKTA LEKSELL STEREOTACTIC SYSTEM WITH MR POST KIT

All identifiers (2)
Aletia (canonical)ALT-001553
FDA 510(k) ยท US (primary)K031999

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K031999
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
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