Cytocorp, Inc.
Country not established
- Devices
- 1
What Cytocorp, Inc. makes
Cytocorp, Inc. manufactures the DIACYTE Fixative Solution, a reagent used in cytopathology for preserving cellular samples during preparation for microscopic examination.
The DIACYTE Fixative Solution is classified as a Class I medical device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Diacyte Fixative Solution Ref K880549
510(k) 510(k)
Frequently asked questions
How many devices does Cytocorp, Inc. have in the registry?
The registry currently lists 1 device for Cytocorp, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cytocorp, Inc.'s devices?
Among its 1 most recently registered device, Cytocorp, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Cytocorp, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cytocorp, Inc.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Cytocorp, Inc. in the registry?
The most recently registered devices listed for Cytocorp, Inc. include DIACYTE FIXATIVE SOLUTION.