Medical Device Manufacturer · US , Hinckley , OH

Cytocolor, Inc.

5 submissions · 5 cleared · Since 1986
5
Total
5
Cleared
0
Denied

Cytocolor, Inc. — FDA 510(k) Submissions

Cytocolor, Inc. has submitted 5 FDA 510(k) premarket notifications since 1986, of which 5 received clearance as substantially equivalent to a predicate device.

The company's most frequent device categories include Stains, Chemical Solution . Use the specialty filter in the sidebar to narrow results.

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