Harding & Harris, Inc.
Country not established
- Devices
- 1
What Harding & Harris, Inc. makes
Harding & Harris, Inc. manufactures automated therapy systems designed for clinical or home-based use, supporting controlled delivery of medical interventions.
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 Therapy System Ref K891693
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Harding & Harris, Inc. have in the registry?
The registry currently lists 1 device for Harding & Harris, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Harding & Harris, Inc.'s devices?
Among its 1 most recently registered device, Harding & Harris, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Harding & Harris, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Harding & Harris, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Harding & Harris, Inc. in the registry?
The most recently registered devices listed for Harding & Harris, Inc. include AUTOMATED THERAPY SYSTEM.