Johari Electro-Tech Co.
IndiaFDA applicant, unverified
- Devices
- 1
What Johari Electro-Tech Co. makes
Johari Electro-Tech Co. manufactures the Analgesic Pulser (Model AP-439), a device designed for transcutaneous electrical nerve stimulation (TENS) to manage pain relief through electrical pulses.
The company’s products are classified under Class II devices in the US and are listed in the FDA’s 510(k) registry. Johari Electro-Tech Co. is based in the United States.
Catalogue
Analgesic Pulser, Model Ap-439 Ref K993229
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Johari Electro-Tech Co. have in the registry?
The registry currently lists 1 device for Johari Electro-Tech Co.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Johari Electro-Tech Co.'s devices?
Among its 1 most recently registered device, Johari Electro-Tech Co. has devices listed in FDA 510(k) (1 device).
What risk classes do Johari Electro-Tech Co.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Johari Electro-Tech Co.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Johari Electro-Tech Co. in the registry?
The most recently registered devices listed for Johari Electro-Tech Co. include ANALGESIC PULSER, MODEL AP-439.