St. Paul Medical
Country not established
- Devices
- 1
What St. Paul Medical makes
St. Paul Medical manufactures the KEY-LOK™ SYSTEM, a medical device designed for vascular access applications, including percutaneous coronary interventions and peripheral vascular procedures.
The KEY-LOK™ SYSTEM is classified as a Class II device under FDA regulations and is listed via the 510(k) pathway. The company is based in the United States.
Catalogue
Key-Lok(Tm) System Ref K940645
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does St. Paul Medical have in the registry?
The registry currently lists 1 device for St. Paul Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list St. Paul Medical's devices?
Among its 1 most recently registered device, St. Paul Medical has devices listed in FDA 510(k) (1 device).
What risk classes do St. Paul Medical's devices fall under?
Among its 1 most recently registered device, the classes recorded for St. Paul Medical's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from St. Paul Medical in the registry?
The most recently registered devices listed for St. Paul Medical include KEY-LOK(TM) SYSTEM.