The following data is part of a premarket notification filed by Esaote, S.p.a. with the FDA for Speedup Software Option.
| Device ID | K120748 |
| 510k Number | K120748 |
| Device Name: | SPEEDUP SOFTWARE OPTION |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | ESAOTE, S.P.A. 9001 Wesleyan Road Suite 200 Indianapolis, IN 46268 |
| Contact | Allison Scott, Rac |
| Correspondent | Allison Scott, Rac ESAOTE, S.P.A. 9001 Wesleyan Road Suite 200 Indianapolis, IN 46268 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-03-12 |
| Decision Date | 2012-05-01 |
| Summary: | summary |