Chroma Vision Medical Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 3
What Chroma Vision Medical Systems, Inc. makes
Chroma Vision Medical Systems, Inc. manufactures the ACIS (Automated Cellular Imaging System), which is a Class II medical device used for automated cellular imaging analysis, along with modifications to this system.
The company is based in the US, and its products are listed in the FDA 510(k) registry, indicating they are Class II devices that have been cleared through the 510(k) notification process.
Catalogue
Acis (Automated Cellular Imaging System) Ref K032113
Regimes: 510(k) Registry: 510(k)Automated Cellular Imaging System (Acis) Ref K984188
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Chroma Vision Medical Systems, Inc. have in the registry?
The registry currently lists 3 devices for Chroma Vision Medical Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Chroma Vision Medical Systems, Inc.'s devices?
Among its 3 most recently registered devices, Chroma Vision Medical Systems, Inc. has devices listed in FDA 510(k) (3 devices).
What risk classes do Chroma Vision Medical Systems, Inc.'s devices fall under?
Among its 3 most recently registered devices, the classes recorded for Chroma Vision Medical Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Chroma Vision Medical Systems, Inc. in the registry?
The most recently registered devices listed for Chroma Vision Medical Systems, Inc. include ACIS (AUTOMATED CELLULAR IMAGING SYSTEM), AUTOMATED CELLULAR IMAGING SYSTEM (ACIS) and MODIFICATION TO ACIS (AUTOMATED CELLULAR IMAGING SYSTEM).