Mark H. Friedman
Country not established
- Devices
- 2
What Mark H. Friedman makes
Mark H. Friedman manufactures the Crytron System, a device designed for cryoablation procedures, and the IVC System, intended for the treatment of venous conditions such as varicose veins. These products are used in minimally invasive medical interventions to address specific vascular and soft tissue concerns.
The company’s portfolio is classified under FDA Class II devices and is recorded in the FDA’s 510(k) premarket notification registry. The manufacturer is based in the United States.
Catalogue
Crytron System Ref K955529
Regimes: 510(k) Registry: 510(k)Ivc System Ref K040317
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mark H. Friedman have in the registry?
The registry currently lists 2 devices for Mark H. Friedman. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mark H. Friedman's devices?
Among its 2 most recently registered devices, Mark H. Friedman has devices listed in FDA 510(k) (2 devices).
What risk classes do Mark H. Friedman's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mark H. Friedman's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mark H. Friedman in the registry?
The most recently registered devices listed for Mark H. Friedman include CRYTRON SYSTEM and IVC SYSTEM.