Peter Lazic GmbH is one of 507 FDA 510(k) medical device manufacturers from Germany in the dataset, ranked by real submission volume.
Peter Lazic GmbH - FDA 510(k) Cleared Devices
Recent clearances: D-Clip, L-ANEURYSM-CLIP SYSTEM & L-ANEURYSM CLIP APPLIERS, YASARGIL ANEURYSM CLIPS & YASARGIL ANEURYSM CLIP APPLIERS
2
Total
2
Cleared
0
Denied
Peter Lazic GmbH has 2 FDA 510(k) cleared medical devices. Based in M?hlheim An Der Donau, DE.
Historical record: 2 cleared submissions from 2008 to 2019. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Peter Lazic GmbH Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Peter Lazic GmbH
2 devices