FDA 510(k) Applications Submitted by QFIX
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K190668 |
03/15/2019 |
Encompass 15 Channel Head Coil, 3T |
Qfix |
K182189 |
08/13/2018 |
Encompass SRS Headframe ; Encompass MR SRS Headframe |
Qfix |
K193243 |
11/25/2019 |
Alta Multipurpose Device |
Qfix |
K171133 |
04/17/2017 |
Qfix« Abdominal/Thoracic Motion Control System,Qfix« SBRT Solution and Accessories |
Qfix |
K230312 |
02/03/2023 |
Iris AirShuttleÖ |
Qfix |
K160627 |
03/07/2016 |
Symphony Patient Transport System, Symphony Patient Trolley, Symphony Standard Transfer Surface, Symphony Portrait (Head/Neck) Transfer Surface, Symphony Brachytherapy solution |
QFIX |
K152321 |
08/17/2015 |
kVue Encompass SRS Insert (Encompass Insert), Encompass SRS Standalone (Encompass Device), Encompass SRS MRI Immobilization device (Encompass MRI Device, Encompass Intracranial Fibreplast Variable Perf Head Only Open View System, Encompass Intracranial Fi |
QFIX |
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