The following data is part of a premarket notification filed by Toshiba Medical Systems Corporation with the FDA for Aquilion Lightning (tsx-035a/2, V7.0).
| Device ID | K151833 |
| 510k Number | K151833 |
| Device Name: | Aquilion Lightning (TSX-035A/2, V7.0) |
| 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 | 2015-07-06 |
| Decision Date | 2015-10-09 |
| Summary: | summary |