FDA 510(k) Applications Submitted by Suzon Lommel
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K190422 |
02/21/2019 |
Viveve System 2.0 |
Viveve Medical |
| K100528 |
02/24/2010 |
BREATHE TECHNOLOGIES VENTILATOR AND ACCESSORIES BT-V2S |
BREATHE TECHNOLOGIES, INC. |
| K150505 |
02/25/2015 |
Cellfina System |
ULTHERA, INC. |
| K180584 |
03/05/2018 |
Viveve RF System, Secure |
Viveve Inc. |
| K121700 |
06/07/2012 |
ULTHERA SYSTEM |
ULTHERA, INC. |
| K132028 |
07/01/2013 |
ULTHERA SYSTEM |
ULTHERA, INC. |
| K161885 |
07/11/2016 |
The Cellfina System |
ULTHERA, INC. |
| K122528 |
08/20/2012 |
ULTHERA SYSTEM |
ULTHERA, INC. |
| K083199 |
10/30/2008 |
CHARTIS CONSOLE |
PULMONX, INC. |
| K153677 |
12/21/2015 |
The Cellfina System |
ULTHERA, INC. |
| K024243 |
12/23/2002 |
REFORM PERIPHERAL CATHETER SYSTEM, MODEL 02200; REFORM PERIPHERAL CATHETERCATHETER, MODEL 02406 |
FOX HOLLOW TECHNOLOGIES |
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