IDEMSA HEMOPHAN HOLLOW FIBER DIALYZERS
Apr 2000
315d
Idemsa
1
Total
1
Cleared
0
Denied
Idemsa — FDA 510(k) Submissions
Idemsa has submitted 1 FDA 510(k) premarket notifications since 2000, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Dialyzer, Capillary, Hollow Fiber . Use the specialty filter in the sidebar to narrow results.
1 devices