Cassandra Electronics Corp.
Country not established
- Devices
- 1
What Cassandra Electronics Corp. makes
Cassandra Electronics Corp. manufactures the AXON II, a dual-channel transcutaneous electrical nerve stimulation (TENS) device designed for pain management applications.
The AXON II is classified as a Class II medical device and is listed under the FDA’s 510(k) pathway. The company is based in the United States.
Catalogue
Axon Ii Brand Of Dual Channel Tens Ref K850860
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Cassandra Electronics Corp. have in the registry?
The registry currently lists 1 device for Cassandra Electronics Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Cassandra Electronics Corp.'s devices?
Among its 1 most recently registered device, Cassandra Electronics Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Cassandra Electronics Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Cassandra Electronics Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Cassandra Electronics Corp. in the registry?
The most recently registered devices listed for Cassandra Electronics Corp. include AXON II BRAND OF DUAL CHANNEL TENS.