The following data is part of a premarket notification filed by Toshiba Medical Systems Corporation with the FDA for Aquilion Lightning, Tsx-036a/1, V8.4.
| Device ID | K170019 |
| 510k Number | K170019 |
| Device Name: | Aquilion Lightning, TSX-036A/1, V8.4 |
| Classification | System, X-ray, Tomography, Computed |
| Applicant | Toshiba Medical Systems Corporation 1385 Shimoishigami Otawara-shi, JP 324-8550 |
| Contact | Paul Biggins |
| Correspondent | Orlando Tadeo Jr. 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 | 2017-01-03 |
| Decision Date | 2017-02-02 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 04987670102608 | K170019 | 000 |