CISBIO RENIN RIA TEST
Mar 2007
248d
Cis Bio International
1
Total
1
Cleared
0
Denied
Cis Bio International — FDA 510(k) Submissions
Cis Bio International has submitted 1 FDA 510(k) premarket notifications since 2007, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Radioimmunoassay, Angiotensin I And Renin . Use the specialty filter in the sidebar to narrow results.
1 devices