C.A.T. DI Corsini G. & C. SpA
ItalyFDA applicant, unverified
- Devices
- 1
What C.A.T. DI Corsini G. & C. SpA makes
C.A.T. DI Corsini G. & C. Spa manufactures the CORSINI 9090, a medical device designed for use in cardiac catheterization procedures, including coronary angiography and percutaneous coronary interventions.
The CORSINI 9090 is classified as a Class II device under FDA regulations and is listed in the FDA’s 510(k) clearance registry. The company is based in the United States.
Catalogue
Corsini 9090 Ref K950402
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does C.A.T. DI Corsini G. & C. Spa have in the registry?
The registry currently lists 1 device for C.A.T. DI Corsini G. & C. Spa. Devices recorded under merged duplicate company entries are counted once.
Which registries list C.A.T. DI Corsini G. & C. Spa's devices?
Among its 1 most recently registered device, C.A.T. DI Corsini G. & C. Spa has devices listed in FDA 510(k) (1 device).
What risk classes do C.A.T. DI Corsini G. & C. Spa's devices fall under?
Among its 1 most recently registered device, the classes recorded for C.A.T. DI Corsini G. & C. Spa's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from C.A.T. DI Corsini G. & C. Spa in the registry?
The most recently registered devices listed for C.A.T. DI Corsini G. & C. Spa include CORSINI 9090.