FLUID LEVEL MONITOR
Apr 2014
125d
Coleman Laboratories
1
Total
1
Cleared
0
Denied
Coleman Laboratories — FDA 510(k) Submissions
Coleman Laboratories has submitted 1 FDA 510(k) premarket notifications since 2014, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Monitor, Electric For Gravity Flow Infusion Systems . Use the specialty filter in the sidebar to narrow results.
1 devices