Medical Device Manufacturer · US , Washington , DC

Sierra Diagnostic, LLC

1 submissions · 1 cleared · Since 2002
1
Total
1
Cleared
0
Denied

Sierra Diagnostic, LLC — FDA 510(k) Submissions

Sierra Diagnostic, LLC has submitted 1 FDA 510(k) premarket notifications since 2002, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Transport, Aerobic . Use the specialty filter in the sidebar to narrow results.

1 devices
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