George H. Frisch
Country not established
- Devices
- 2
What George H. Frisch makes
George H. Frisch manufactures transcutaneous nerve stimulators, including models like the MENTOR 150 and MENTOR 402, which deliver electrical stimulation through the skin for therapeutic purposes.
These devices are classified as Class II under FDA regulations and are listed via the 510(k) clearance process. The company is based in the United States.
Catalogue
Mentor 150 Transcutaneous Nerve Stimula Ref K803121
Regimes: 510(k) Registry: 510(k)Mentor 402 Transcutaneous Elec. Stimulat Ref K803113
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does George H. Frisch have in the registry?
The registry currently lists 2 devices for George H. Frisch. Devices recorded under merged duplicate company entries are counted once.
Which registries list George H. Frisch's devices?
Among its 2 most recently registered devices, George H. Frisch has devices listed in FDA 510(k) (2 devices).
What risk classes do George H. Frisch's devices fall under?
Among its 2 most recently registered devices, the classes recorded for George H. Frisch's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from George H. Frisch in the registry?
The most recently registered devices listed for George H. Frisch include MENTOR 150 TRANSCUTANEOUS NERVE STIMULA and MENTOR 402 TRANSCUTANEOUS ELEC. STIMULAT.