Medical Device Manufacturer · US , Baltimore , MD

Personal Genome Diagnostics

1 submissions · 1 cleared · Since 2020
1
Total
1
Cleared
0
Denied

Personal Genome Diagnostics — FDA 510(k) Submissions

Personal Genome Diagnostics has submitted 1 FDA 510(k) premarket notifications since 2020, of which 1 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Next Generation Sequencing Based Tumor Profiling Test . Use the specialty filter in the sidebar to narrow results.

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