Medical Device Manufacturer · IE , Ballina

Technopath Manufacturing

1 submissions · 1 cleared · Since 2016
1
Total
1
Cleared
0
Denied

Technopath Manufacturing — FDA 510(k) Submissions

Technopath Manufacturing has submitted 1 FDA 510(k) premarket notifications since 2016, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Single (specified) Analyte Controls (assayed And Unassayed) . Use the specialty filter in the sidebar to narrow results.

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