FDA 510(k) Applications Submitted by Brad Renton
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K180709 |
03/19/2018 |
truSculpt RF Device; truSculpt; truSculpt 3D |
Cutera, Inc. |
| K992298 |
07/08/1999 |
IRIDERM, MODEL APEX 800 |
IRIDEX CORP. |
| K160488 |
02/22/2016 |
Cutera enlighten III Laser System |
Cutera, Inc. |
| K140727 |
03/24/2014 |
CUTERA PICOSECOND LASER SYSTEM |
CUTERA, INC. |
| K170936 |
03/30/2017 |
Cutera enlighten III Laser System |
Cutera, Inc. |
| K172004 |
07/03/2017 |
truSculpt |
Cutera, Inc. |
| K172077 |
07/10/2017 |
Cutera enlighten III Laser System |
Cutera, Inc. |
| K162512 |
09/08/2016 |
truSculpt |
CUTERA, INC. |
| K133739 |
12/09/2013 |
TRUSCULPT |
CUTERA, INC. |
| K133945 |
12/23/2013 |
CUTERA PICOSECOND LASER SYSTEM |
CUTERA, INC. |
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