Medical Device Manufacturer · US , Huntsville , AL

Icubate, Inc.

2 submissions · 2 cleared · Since 2017
2
Total
2
Cleared
0
Denied

Icubate, Inc. — FDA 510(k) Submissions

Icubate, Inc. has submitted 2 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 Gram-positive Bacteria And Their Resistance Markers, Gram-negative Bacteria And Associated Resistance Markers . Use the specialty filter in the sidebar to narrow results.

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All2 Microbiology 2