Medical Device Manufacturer · US , Beverly , MA

Seegene

1 submissions · 1 cleared · Since 2015
1
Total
1
Cleared
0
Denied

Seegene — FDA 510(k) Submissions

Seegene has submitted 1 FDA 510(k) premarket notifications since 2015, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Herpes Simplex Virus Nucleic Acid Amplification Assay . Use the specialty filter in the sidebar to narrow results.

1 devices
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