Medical Device Manufacturer · US , Irvine , CA

Fertipro NV

4 submissions · 4 cleared · Since 2006
4
Total
4
Cleared
0
Denied

Fertipro NV — FDA 510(k) Submissions

Fertipro NV has submitted 4 FDA 510(k) premarket notifications since 2006, of which 4 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Media, Reproductive, Microbial Nucleic Acid Storage And Stabilization Device . Use the specialty filter in the sidebar to narrow results.

4 devices
1–4 of 4
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All4 Obstetrics & Gynecology 3 Microbiology 1