FDA 510(k) Applications Submitted by CATHERINE RIPLE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K021337 |
04/26/2002 |
AART PECTORALIS IMPLANT |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K021417 |
05/03/2002 |
AART CHIN IMPLANT |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K021418 |
05/03/2002 |
AART NASAL IMPLANT |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K021419 |
05/03/2002 |
AART MALAR IMPLANT |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K021820 |
06/04/2002 |
AART SILICONE CARVING BLOCK |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K021839 |
06/04/2002 |
AART GLUTEAL IMPLANT |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K982051 |
06/11/1998 |
KELOCATE SHEETING |
ALLIED BIOMEDICAL CORP. |
K022223 |
07/09/2002 |
AART SILICONE SHEETING |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K022306 |
07/16/2002 |
AART SILICONE TUBING |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K022511 |
07/30/2002 |
AART CALF IMPLANT |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
K023678 |
11/01/2002 |
DIMISIL SCAR GEL |
AESTHETIC AND RECONSTRUCTIVE TECHNOLOGIES, INC. |
|
|