TOTAL CONTAINMENT DEVICE
May 1994
1023d
Denco
1
Total
1
Cleared
0
Denied
Denco — FDA 510(k) Submissions
Denco has submitted 1 FDA 510(k) premarket notifications since 1994, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Dialysate Delivery, Semi-automatic, Peritoneal . Use the specialty filter in the sidebar to narrow results.
1 devices