The following data is part of a premarket notification filed by Toshiba Medical Systems Corporation with the FDA for Vantage Elan 1.5t, V4.0.
Device ID | K171597 |
510k Number | K171597 |
Device Name: | Vantage Elan 1.5T, V4.0 |
Classification | System, Nuclear Magnetic Resonance Imaging |
Applicant | Toshiba Medical Systems Corporation 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 | LNH |
CFR Regulation Number | 892.1000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-05-31 |
Decision Date | 2017-07-21 |
Summary: | summary |