K122613Substantially Equivalent
Vantage Titan with Helios Gradient Model Mrt-1504/Us
Toshiba America Medical Systems, In.C, Tustin CA / Traditional, Substantially Equivalent
K122613 is the FDA 510(k) clearance record for VANTAGE TITAN WITH HELIOS GRADIENT MODEL MRT-1504/US, a class II device, cleared for Toshiba America Medical Systems, In.C on under FDA product code LNH (System, Nuclear Magnetic Resonance Imaging). FDA records list 146 510(k) clearances for Toshiba America Medical Systems, In.C, from to . As of , FDA records show 3 recalls naming K122613.
Clearance record
- Decision date
- Received
- (108 days to decision)
- Product code
- LNH System, Nuclear Magnetic Resonance Imaging
- Regulation
- 21 CFR 892.1000
- Device class
- Class II
- Review panel
- Radiology
- Applicant
- Toshiba America Medical Systems, In.C 2441 Michelle Dr., Tustin CA
- 510(k) summary
- Summary PDF
- Third party review
- No
Clearances, product code LNH
Trailing 12 monthsShow the numbers
| Month | Clearances |
|---|---|
| November 2025 | 1 |
| December 2025 | 3 |
| January 2026 | 1 |
| February 2026 | 4 |
| March 2026 | 6 |
| April 2026 | 1 |
| May 2026 | 1 |
| June 2026 | 0 |
| July 2026 | 2 |
| August 2026 | 3 |
| September 2026 | 3 |
| October 2026 | 0 |
FIRST ARTICLE / WEEKLY
What cleared, what was recalled, and what changed in the standards. One edition a week for the people who make medical devices.
