Medical Device Manufacturer · AU , Australia

Benchmark Reagents

1 submissions · 1 cleared · Since 1987
1
Total
1
Cleared
0
Denied

Benchmark Reagents — FDA 510(k) Submissions

Benchmark Reagents 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 Resin, Ion-exchange, Ascorbic Acid, Colorimetry, Iron Binding Capacity . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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