COAGCARE ANTICOAGULATION MANAGEMENT SYSTEM
Aug 2005
138d
Zycare
1
Total
1
Cleared
0
Denied
Zycare — FDA 510(k) Submissions
Zycare has submitted 1 FDA 510(k) premarket notifications since 2005, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Instrument, Coagulation . Use the specialty filter in the sidebar to narrow results.
1 devices