IndexMethodologyInsightsFor CliniciansRequest Review
Index/Catheter Precision, Inc.
ALT-003516K183195Amber Status

VIVO

Catheter Precision, Inc. ยท Manufacturer

All identifiers (2)
Aletia (canonical)ALT-003516
FDA 510(k) ยท US (primary)K183195

Regulatory Registrations

๐ŸŒ
US
FDA
ID: K183195
510k

Lifecycle Signals

Last Automated Sync
Mar 2026
Last Clinical Review
Not reviewed
This listing was auto-populated from public registry data
Some fields are incomplete or unverified. If you represent Catheter Precision, Inc., you can verify and update this listing.
Verify this listing โ†’
โ† Back to Index