Dba Systems, Inc.
United StatesFDA applicant, unverified
- Devices
- 2
What Dba Systems, Inc. makes
Dba Systems, Inc. manufactures the IMAGCLEAR Mammography Review System, a digital tool designed for post-processing and enhancing mammographic images to improve diagnostic clarity. The company also produces the DFS-2100, a device intended for digital film scanning and archiving in radiology workflows.
These devices are classified as Class II under FDA regulations and are supported by 510(k) clearance pathways. The company is based in the United States.
Catalogue
Imagclear Mammography Review System Ref K992467
Regimes: 510(k) Registry: 510(k)Dfs-2100 Ref K932760
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Dba Systems, Inc. have in the registry?
The registry currently lists 2 devices for Dba Systems, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Dba Systems, Inc.'s devices?
Among its 2 most recently registered devices, Dba Systems, Inc. has devices listed in FDA 510(k) (2 devices).
What risk classes do Dba Systems, Inc.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Dba Systems, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Dba Systems, Inc. in the registry?
The most recently registered devices listed for Dba Systems, Inc. include IMAGCLEAR MAMMOGRAPHY REVIEW SYSTEM and DFS-2100.