Medical Device Manufacturer · IL , Rehovot

Nucleix , Ltd.

1 submissions · 1 cleared · Since 2023
1
Total
1
Cleared
0
Denied

Nucleix , Ltd. — FDA 510(k) Submissions

Nucleix , Ltd. has submitted 1 FDA 510(k) premarket notifications since 2023, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Tumor Marker, Monitoring, Bladder . Use the specialty filter in the sidebar to narrow results.

1 devices
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