The following data is part of a premarket notification filed by C.a.t. Di Corsini G. & C. Spa with the FDA for Corsini 9090.
| Device ID | K950402 |
| 510k Number | K950402 |
| Device Name: | CORSINI 9090 |
| Classification | Table, Radiographic, Tilting |
| Applicant | C.A.T. DI CORSINI G. & C. SPA VIA PILA 3/3 40044 - Pontecchio Marconi(bo), IT 40044 |
| Contact | Francesco Bianco |
| Correspondent | Francesco Bianco C.A.T. DI CORSINI G. & C. SPA VIA PILA 3/3 40044 - Pontecchio Marconi(bo), IT 40044 |
| Product Code | IXR |
| CFR Regulation Number | 892.1980 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-02-01 |
| Decision Date | 1995-03-31 |