FreeStyle InsuLinx Blood Glucose Monotioring System
Sep 2015
30d
Abott Laboratories
1
Total
1
Cleared
0
Denied
Abott Laboratories — FDA 510(k) Submissions
Abott Laboratories has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Glucose Dehydrogenase, Glucose . Use the specialty filter in the sidebar to narrow results.
1 devices