Medical Device Manufacturer · US , Sparks , MD

Trimgen Corporation

1 submissions · 1 cleared · Since 2009
1
Total
1
Cleared
0
Denied

Trimgen Corporation — FDA 510(k) Submissions

Trimgen Corporation has submitted 1 FDA 510(k) premarket notifications since 2009, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Cytochrome P450 2c9 (cyp450 2c9) Drug Metabolizing Enzyme Genotyping System . Use the specialty filter in the sidebar to narrow results.

1 devices
1–1 of 1
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All1 Toxicology 1