ALT-007196K120489Green Status
TISSUE OF ORIGIN TEST KIT FFPE
PATHWORK DIAGNOSTICS, INC. ยท Manufacturer
All identifiers (2)
Aletia (canonical)
ALT-007196FDA 510(k) ยท US (primary)
K120489Overview
Specialty
Pathology
Accountability Tier
Tier 2
Regulatory Registrations
๐
US
FDA
ID: K120489
510k
Lifecycle Signals
Last Automated Sync
Jun 2026
Last Clinical Review
Not reviewed
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Some fields are incomplete or unverified. If you represent PATHWORK DIAGNOSTICS, INC., you can verify and update this listing.
