NEOCARE 20 MICRON BLOOD FILTER
May 2000
88d
Whatman, Inc.
1
Total
1
Cleared
0
Denied
Whatman, Inc. — FDA 510(k) Submissions
Whatman, Inc. 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 Microfilter, Blood Transfusion . Use the specialty filter in the sidebar to narrow results.
1 devices