Anritsu America Co.
Country not established
- Devices
- 2
What Anritsu America Co. makes
Anritsu America Co. manufactures transcutaneous electrical nerve stimulation (TENS) devices, including the TENSMAX and HEALTH POINT models, designed for pain management and muscle stimulation therapy.
These devices are regulated as Class II and Unclassified (Class U) under FDA 510(k) clearance requirements. The company’s products are listed in the FDA’s 510(k) registry, and the manufacturer is based in the United States.
Catalogue
Tensmax Ref K811499
Regimes: 510(k) Registry: 510(k)Health Point Ref K781651
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Anritsu America Co. have in the registry?
The registry currently lists 2 devices for Anritsu America Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Anritsu America Co.'s devices?
Among its 2 most recently registered devices, Anritsu America Co. has devices listed in FDA 510(k) (2 devices).
What risk classes do Anritsu America Co.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Anritsu America Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Anritsu America Co. in the registry?
The most recently registered devices listed for Anritsu America Co. include TENSMAX and HEALTH POINT.