PCTE MICROPOROUS MEMBRANE FILTER
May 1987
112d
Poretics Corp.
1
Total
1
Cleared
0
Denied
Poretics Corp. — FDA 510(k) Submissions
Poretics Corp. has submitted 1 FDA 510(k) premarket notifications since 1987, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Filters, Cell Collection, Tissue Processing . Use the specialty filter in the sidebar to narrow results.
1 devices