Nanopac, Inc.
Country not established
- Devices
- 1
What Nanopac, Inc. makes
Nanopac, Inc. manufactures the CINTEX, a medical device designed for specific diagnostic or procedural applications in radiology or interventional cardiology, such as contrast-enhanced imaging or catheter-based interventions.
The CINTEX 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
Cintex Ref K903605
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nanopac, Inc. have in the registry?
The registry currently lists 1 device for Nanopac, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nanopac, Inc.'s devices?
Among its 1 most recently registered device, Nanopac, Inc. has devices listed in FDA 510(k) (1 device).
What risk classes do Nanopac, Inc.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Nanopac, Inc.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Nanopac, Inc. in the registry?
The most recently registered devices listed for Nanopac, Inc. include CINTEX.