Medical Device Manufacturer · US , Baldwin , MD

Geneohm Sciences Canada, Inc.

2 submissions · 2 cleared · Since 2006
2
Total
2
Cleared
0
Denied

Geneohm Sciences Canada, Inc. — FDA 510(k) Submissions

Geneohm Sciences Canada, Inc. has submitted 2 FDA 510(k) premarket notifications since 2006, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include System, Test, Genotypic Detection, Resistant Markers, Enterococcus Species, System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen . Use the specialty filter in the sidebar to narrow results.

2 devices
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