CKHEMO, MODEL CKHEMO VERSION 1.0
Nov 1999
147d
Csam, Inc.
1
Total
1
Cleared
0
Denied
Csam, Inc. — FDA 510(k) Submissions
Csam, Inc. has submitted 1 FDA 510(k) premarket notifications since 1999, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include System, Dialysate Delivery, Single Patient . Use the specialty filter in the sidebar to narrow results.
1 devices