Globalcare/Bay Medical Corp.
Country not established
- Devices
- 1
What Globalcare/Bay Medical Corp. makes
Globalcare/Bay Medical Corp. manufactures the TX 3 TENS Modified, a transcutaneous electrical nerve stimulation (TENS) device designed for pain management applications.
The TX 3 TENS Modified 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
Tx 3 Tens Modified Ref K913532
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Globalcare/Bay Medical Corp. have in the registry?
The registry currently lists 1 device for Globalcare/Bay Medical Corp.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Globalcare/Bay Medical Corp.'s devices?
Among its 1 most recently registered device, Globalcare/Bay Medical Corp. has devices listed in FDA 510(k) (1 device).
What risk classes do Globalcare/Bay Medical Corp.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Globalcare/Bay Medical Corp.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Globalcare/Bay Medical Corp. in the registry?
The most recently registered devices listed for Globalcare/Bay Medical Corp. include TX 3 TENS MODIFIED.