The following data is part of a premarket notification filed by Toshiba Medical Systems Corporation with the FDA for Aquilion One (tsx-305a/3) V8.3 With First 2.1.
| Device ID | K170177 |
| 510k Number | K170177 |
| Device Name: | Aquilion ONE (TSX-305A/3) V8.3 With FIRST 2.1 |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Toshiba Medical Systems Corporation 1385 Shimoishigami Otawara-shi, JP 324-8550 |
| Contact | Paul Biggins |
| Correspondent | Orlando Tadeo Toshiba America Medical Systems, Inc. 2441 Michelle Drive Tustin, CA 92780 |
| Product Code | JAK |
| CFR Regulation Number | 892.1750 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-01-19 |
| Decision Date | 2017-06-30 |
| Summary: | summary |