Nexcore GI Insufflator
Sep 2016
41d
Nexcore Technology, LLC
1
Total
1
Cleared
0
Denied
Nexcore Technology, LLC — FDA 510(k) Submissions
Nexcore Technology, LLC has submitted 1 FDA 510(k) premarket notifications since 2016, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Insufflator, Automatic Carbon-dioxide For Endoscope . Use the specialty filter in the sidebar to narrow results.
1 devices