FDA 510(k) Applications Submitted by Corinth MedTech, Inc.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K230205 |
01/25/2023 |
Veloxion System |
Corinth MedTech, Inc. |
| K190099 |
01/22/2019 |
Veloxion Controller Kit, Veloxion Fluid Control Kit, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch |
Corinth MedTech, Inc. |
| K190113 |
01/24/2019 |
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags |
Corinth MedTech, Inc. |
| K180752 |
03/22/2018 |
Veloxion System, Veloxion Controller Kit, Veloxion Resecting Device Kit, Veloxion Fluid Control Set, Veloxion Saline Pole |
Corinth MedTech, Inc. |
| K191335 |
05/17/2019 |
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags |
Corinth MedTech, Inc. |
| K191341 |
05/20/2019 |
Veloxion Controller Kit, Veloxion Fluid Control Set, Veloxion Resectoscope, Veloxion Video Control Unit, Veloxion Roll Stand, Waste Management Tubing, Tissue Catch, Waste Management Bags |
Corinth MedTech, Inc. |
| K162979 |
10/26/2016 |
Veloxion System |
Corinth MedTech, Inc. |
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