The following data is part of a premarket notification filed by Esaote S.p.a. with the FDA for 6200 Ultrasound System And 6250 Ultrasound System.
| Device ID | K153277 |
| 510k Number | K153277 |
| Device Name: | 6200 Ultrasound System And 6250 Ultrasound System |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | Esaote S.p.A. Via Siffredi 58 Genovo, IT 16153 |
| Contact | Donatella Ragghianti |
| Correspondent | Allison Scott Navigant Consulting, Inc 9001 Wesleyan Road, 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 | 2015-11-12 |
| Decision Date | 2016-05-04 |
| Summary: | summary |