OMNYX IDP FOR HER2 MANUAL APPLICATION
Apr 2014
344d
Omnyx, LLC
1
Total
1
Cleared
0
Denied
Omnyx, LLC — FDA 510(k) Submissions
Omnyx, LLC 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 Automated Digital Image Manual Interpretation Microscope . Use the specialty filter in the sidebar to narrow results.
1 devices