i3 ONE (203100-S);i3 TWO connect (203200-S);i3 TWO direct (203300-S)
Jun 2023
267d
I3 Membrane GmbH
1
Total
1
Cleared
0
Denied
I3 Membrane GmbH — FDA 510(k) Submissions
I3 Membrane GmbH 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, Water Purification, General Medical Use . Use the specialty filter in the sidebar to narrow results.
1 devices