Woodson and Associates, LLC
United StatesFDA applicant, unverified
- Devices
- 2
What Woodson and Associates, LLC makes
Woodson and Associates, LLC produces automated medical report generation systems, including software tools like the Automated Medical Report Writer and The Osteoreport, designed to assist in creating structured medical documentation.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Automated Medical Report Writer Ref K981553
Regimes: 510(k) Registry: 510(k)The Osteoreport Ref K934040
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Woodson and Associates, LLC have in the registry?
The registry currently lists 2 devices for Woodson and Associates, LLC. Devices recorded under merged duplicate company entries are counted once.
Which registries list Woodson and Associates, LLC's devices?
Among its 2 most recently registered devices, Woodson and Associates, LLC has devices listed in FDA 510(k) (2 devices).
What risk classes do Woodson and Associates, LLC's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Woodson and Associates, LLC's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Woodson and Associates, LLC in the registry?
The most recently registered devices listed for Woodson and Associates, LLC include AUTOMATED MEDICAL REPORT WRITER and THE OSTEOREPORT.