Fulcrum Medical, Inc.
Country not established
- Devices
- 1
What Fulcrum Medical, Inc. makes
Fulcrum Medical, Inc. manufactures the FULACCESS Model 1.0, a medical device designed for vascular access procedures.
The FULACCESS Model 1.0 is classified as a Class II device under FDA regulations and is listed in the 510(k) clearance registry. The company is based in the United States.
Catalogue
Fulaccess Model 1.0 Ref K101707
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Fulcrum Medical, Inc. have in the registry?
The registry currently lists 1 device for Fulcrum Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Fulcrum Medical, Inc.'s devices?
Among its 1 most recently registered device, Fulcrum Medical, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Fulcrum Medical, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Fulcrum Medical, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Fulcrum Medical, Inc. in the registry?
The most recently registered devices listed for Fulcrum Medical, Inc. include FULACCESS MODEL 1.0.