Medical Device Manufacturer · US , Palo Alto , CA

Id-Fish Technology, Inc.

3 submissions · 2 cleared · Since 2017
3
Total
2
Cleared
1
Denied

Id-Fish Technology, Inc. — FDA 510(k) Submissions

Id-Fish Technology, Inc. has submitted 3 FDA 510(k) premarket notifications since 2017, of which 2 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Reagent, Borrelia Serological Reagent, Fish (fluorescence In Situ Hybridization) Kit, Nucleic Acid, Plasmodium Sp. . Use the specialty filter in the sidebar to narrow results.

3 devices
1–3 of 3
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All3 Microbiology 3