The following data is part of a premarket notification filed by Canon Medical Systems Corporation with the FDA for Vantage Titan 3t, Mrt-3010, V2.5.
| Device ID | K191128 |
| 510k Number | K191128 |
| Device Name: | Vantage Titan 3T, MRT-3010, V2.5 |
| Classification | System, Nuclear Magnetic Resonance Imaging |
| Applicant | Canon Medical Systems Corporation 1385 Shimoishigami Otawara-shi, JP 324-8550 |
| Contact | Paul Biggins |
| Correspondent | Orlando Tadeo Canon Medical Systems USA, Inc. 2441 Michelle Drive Tustin, CA 92780 |
| Product Code | LNH |
| CFR Regulation Number | 892.1000 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2019-04-29 |
| Decision Date | 2019-06-26 |