MILLICORE AB DIGIVENT CHEST DRAINAGE SYSTEM
Oct 2006
59d
Millicore AB
1
Total
1
Cleared
0
Denied
Millicore AB — FDA 510(k) Submissions
Millicore AB has submitted 1 FDA 510(k) premarket notifications since 2006, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Bottle, Collection, Vacuum . Use the specialty filter in the sidebar to narrow results.
1 devices