The following data is part of a premarket notification filed by Canon Medical Systems Corporation with the FDA for Aquilion Precision (tsx-304a/1 And /2) V8.8 With Aice.
| Device ID | K182901 |
| 510k Number | K182901 |
| Device Name: | Aquilion Precision (TSX-304A/1 And /2) V8.8 With AiCE |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Canon Medical Systems Corporation 1385 Shimoishigami Otawara-shi, JP 324-8550 |
| Contact | Paul Biggins |
| Correspondent | Orlando Tadeo Jr. Canon Medical Systems Corporation 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 | 2018-10-16 |
| Decision Date | 2019-07-05 |