ELECTR-TRANSBLOTTER
Jan 1989
220d
The W.E.P. Co.
1
Total
1
Cleared
0
Denied
The W.E.P. Co. — FDA 510(k) Submissions
The W.E.P. Co. has submitted 1 FDA 510(k) premarket notifications since 1989, of which 1 received clearance as substantially equivalent to a predicate device.
The company's most frequent device categories include Apparatus, Electrophoresis, For Clinical Use . Use the specialty filter in the sidebar to narrow results.
1 devices