Clearview Diagnostics, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Clearview Diagnostics, Inc. makes
Clearview Diagnostics, Inc. manufactures medical imaging devices, including the CLEARVIEWHD for high-definition imaging and the ClearView cCAD for computer-aided detection in diagnostic radiology, primarily for breast imaging.
The company’s portfolio is regulated under FDA Class II devices, with products authorised via the 510(k) clearance pathway. These devices are listed in the FDA’s 510(k) database. The manufacturer is based in the United States.
Catalogue
Clearviewhd Ref K140139
Regimes: 510(k) Registry: 510(k)ClearView cCAD Ref K161959
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Clearview Diagnostics, Inc. have in the registry?
The registry currently lists 2 devices for Clearview Diagnostics, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Clearview Diagnostics, Inc.'s devices?
Among its 2 most recently registered devices, Clearview Diagnostics, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Clearview Diagnostics, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Clearview Diagnostics, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Clearview Diagnostics, Inc. in the registry?
The most recently registered devices listed for Clearview Diagnostics, Inc. include CLEARVIEWHD and ClearView cCAD.