FDA 510(k) Applications Submitted by Beka Vite
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K180088 |
01/12/2018 |
TrapLiner catheter |
Vascular Solutions, Inc. |
| K151234 |
05/08/2015 |
R350 guidewire |
VASCULAR SOLUTIONS, INC. |
| K171335 |
05/08/2017 |
Venture 038 catheter |
Vascular Solutions, Inc. |
| K191560 |
06/13/2019 |
Turnpike Catheter; Turnpike Spiral Catheter; Turnpike Gold Catheter; Turnpike LP Catheter |
Vascular Solutions LLC |
| K161702 |
06/20/2016 |
Endura guidewire |
Vascular Solutions, Inc. |
| K161901 |
07/11/2016 |
TrapLiner catheter |
Vascular Solutions, Inc. |
| K172090 |
07/11/2017 |
GuideLiner V3 Catheter |
Vascular Solutions, Inc. |
| K212167 |
07/12/2021 |
R350 guidewire, Spectre guidewire, Raider guidewire, Bandit guidewire, Warrior guidewire |
Vascular Solutions LLC |
| K151981 |
07/17/2015 |
Turnpike catheter |
VASCULAR SOLUTION, INC. |
| K162272 |
08/12/2016 |
Fluent inflation device |
VASCULAR SOLUTIONS, INC. |
| K152387 |
08/24/2015 |
Fluent Inflation Device |
VASCULAR SOLUTIONS, INC. |
| K173532 |
11/15/2017 |
Raider Guidewire |
Vascular Solutions, Inc. |
| K163444 |
12/08/2016 |
Spectre guidewire |
Vascular Solutions, Inc. |
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