The following data is part of a premarket notification filed by Toshiba Medical Systems Coroporation with the FDA for Infinix Infx-8000v, V6.40.
| Device ID | K170909 |
| 510k Number | K170909 |
| Device Name: | Infinix INFX-8000V, V6.40 |
| Classification | Interventional Fluoroscopic X-ray System |
| Applicant | Toshiba Medical Systems Coroporation 1385 Shimoishigami Otawara-shi, JP 324-8550 |
| Contact | Paul Biggins |
| Correspondent | Paul Biggins Toshiba America Medical Systems, Inc. 2441 Michelle Drive Tustin, CA 92780 |
| Product Code | OWB |
| Subsequent Product Code | IZI |
| Subsequent Product Code | JAA |
| CFR Regulation Number | 892.1650 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-03-28 |
| Decision Date | 2017-06-16 |
| Summary: | summary |