The following data is part of a premarket notification filed by Esaote S.p.a. with the FDA for Mylabseven 6400, Mylabalpha 7400.
| Device ID | K132466 |
| 510k Number | K132466 |
| Device Name: | MYLABSEVEN 6400, MYLABALPHA 7400 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | ESAOTE S.P.A. 9001 WESLEYAN RD. SUITE 200 Indianapolis, IN 46268 |
| Contact | Allison Scott |
| Correspondent | Allison Scott ESAOTE S.P.A. 9001 WESLEYAN RD. SUITE 200 Indianapolis, IN 46268 |
| Product Code | IYN |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-08-07 |
| Decision Date | 2013-12-04 |
| Summary: | summary |