Laralab GmbH - FDA 510(k) Cleared Devices
1
Total
1
Cleared
0
Denied
Laralab GmbH has 1 FDA 510(k) cleared medical devices. Based in Munich, DE.
Latest FDA clearance: Apr 2025. Active since 2025. Primary specialty: Radiology.
Browse the FDA 510(k) cleared devices submitted by Laralab GmbH Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Hogan Lovells US LLP as regulatory consultant.
1 devices