The following data is part of a premarket notification filed by Hitachi Healthcare Americas Corporation with the FDA for Aloka Arietta 850.
| Device ID | K173739 |
| 510k Number | K173739 |
| Device Name: | ALOKA ARIETTA 850 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | Hitachi Healthcare Americas Corporation 1959 Summit Commerce Park Twinsburg, OH 44087 |
| Contact | Doug Thistlethwaite |
| Correspondent | Doug Thistlethwaite Hitachi Healthcare Americas Corporation 1959 Summit Commerce Park Twinsburg, OH 44087 |
| Product Code | IYN |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-12-07 |
| Decision Date | 2018-02-28 |
| Summary: | summary |