Medical Device Manufacturer · US , Eden Prairie , MN

Lasag AG

2 submissions · 2 cleared · Since 1989
2
Total
2
Cleared
0
Denied

Lasag AG — FDA 510(k) Submissions

Lasag AG has submitted 2 FDA 510(k) premarket notifications since 1989, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Laser, Neodymium:yag, Ophthalmic For Posterior Capsulotomy And Cutting Pupilla, Laser, Ophthalmic . Use the specialty filter in the sidebar to narrow results.

2 devices
1–2 of 2
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