U.S. Clinical Products, Inc.
Country not established
- Devices
- 1
What U.S. Clinical Products, Inc. makes
U.S. Clinical Products, Inc. manufactures the IVA SEAL II, a device designed for securing intravenous access ports to reduce contamination risk and improve patient safety during medical procedures.
The IVA SEAL II is classified as a Class II medical device under U.S. regulations and is listed in the FDA’s 510(k) registry. The company operates from the United States.
Catalogue
Iva Seal Ii Ref K812527
510(k) 510(k)
Frequently asked questions
How many devices does U.S. Clinical Products, Inc. have in the registry?
The registry currently lists 1 device for U.S. Clinical Products, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list U.S. Clinical Products, Inc.'s devices?
Among its 1 most recently registered device, U.S. Clinical Products, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do U.S. Clinical Products, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for U.S. Clinical Products, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from U.S. Clinical Products, Inc. in the registry?
The most recently registered devices listed for U.S. Clinical Products, Inc. include IVA SEAL II.