ESENSOR WARFARIN SENSITIVITY SALIVA TEST
Dec 2011
255d
GenMark Diagnostics, Inc.
1
Total
1
Cleared
0
Denied
GenMark Diagnostics, Inc. — FDA 510(k) Submissions
GenMark Diagnostics, Inc. has submitted 1 FDA 510(k) premarket notifications since 2011, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Instrumentation For Clinical Multiplex Test Systems . Use the specialty filter in the sidebar to narrow results.
1 devices