James J. Schramm
Country not established
- Devices
- 1
What James J. Schramm makes
James J. Schramm manufactures I.V. Start Kits, which are sterile, single-use devices designed for initiating intravenous access in clinical settings.
These products are regulated as Class II medical devices under FDA 510(k) clearance requirements and are listed in the FDA’s 510(k) database. The company operates from the United States.
Catalogue
I.V. Start Kit Ref K950686
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does James J. Schramm have in the registry?
The registry currently lists 1 device for James J. Schramm. Devices recorded under merged duplicate company entries are counted once.
Which registries list James J. Schramm's devices?
Among its 1 most recently registered device, James J. Schramm has devices listed in FDA 510(k) (1 device).
What risk classes do James J. Schramm's devices fall under?
Among its 1 most recently registered device, the classes recorded for James J. Schramm's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from James J. Schramm in the registry?
The most recently registered devices listed for James J. Schramm include I.V. START KIT.