Medical Device Manufacturer · DE , M?hlheim An Der Donau

Peter Lazic GmbH

2 submissions · 2 cleared · Since 2008
2
Total
2
Cleared
0
Denied

Peter Lazic GmbH — FDA 510(k) Submissions

Peter Lazic GmbH has submitted 2 FDA 510(k) premarket notifications since 2008, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Clip, Aneurysm . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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All2 Neurology 2