Mark-Clark
Country not established
- Devices
- 2
What Mark-Clark makes
Mark-Clark manufactures medical devices including the BODY BOOT and CATH CADDIE, which are designed for specific medical applications.
The company's products are regulated as Class I and Class II medical devices and are listed in the FDA 510(k) registry. Mark-Clark is based in the US.
Catalogue
Body Boot Ref K940723
Regimes: 510(k) Registry: 510(k)Cath Caddie Ref K961884
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Mark-Clark have in the registry?
The registry currently lists 2 devices for Mark-Clark. Devices recorded under merged duplicate company entries are counted once.
Which registries list Mark-Clark's devices?
Among its 2 most recently registered devices, Mark-Clark has devices listed in FDA 510(k) (2 devices).
What risk classes do Mark-Clark's devices fall under?
Among its 2 most recently registered devices, the classes recorded for Mark-Clark's devices are Class I and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Mark-Clark in the registry?
The most recently registered devices listed for Mark-Clark include BODY BOOT and CATH CADDIE.