PERIO-TEST
Jul 1987
31d
Dr. Bernard Loewenthal
1
Total
1
Cleared
0
Denied
Dr. Bernard Loewenthal — FDA 510(k) Submissions
Dr. Bernard Loewenthal 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 Gauge, Depth, Instrument, Dental . Use the specialty filter in the sidebar to narrow results.
1 devices