FDA 510(k) Applications Submitted by HANSON MEDICAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040307 |
02/09/2004 |
HANSON SCAR ADE |
HANSON MEDICAL, INC. |
| K973572 |
09/19/1997 |
KELOCOTE SCAR GEL AND KELOCOTE LASER GEL |
HANSON MEDICAL, INC. |
| K973574 |
09/19/1997 |
DURALASTIC ANATOMICAL MALAR IMPLANT |
HANSON MEDICAL, INC. |
| K973575 |
09/19/1997 |
DURALASTIC ANATOMICAL CHIN IMPLANTS |
HANSON MEDICAL, INC. |
| K973728 |
09/30/1997 |
SILICONE CARVING BLOCK |
HANSON MEDICAL, INC. |
| K973729 |
09/30/1997 |
POWERFLEX PEC IMPLANT |
HANSON MEDICAL, INC. |
| K090803 |
03/24/2009 |
HANSON MEDICAL FACIAL IMPLANTS |
HANSON MEDICAL, INC. |
| K071018 |
04/10/2007 |
MONARCH NASAL IMPLANT |
HANSON MEDICAL, INC. |
| K041690 |
06/22/2004 |
MONARCH NASAL IMPLANT |
HANSON MEDICAL, INC. |
| K973730 |
09/30/1997 |
DURASIL I AND DURASIL II |
HANSON MEDICAL, INC. |
| K973573 |
09/19/1997 |
DURALASTIC ANATOMICAL NASAL IMPLANTS |
HANSON MEDICAL, INC. |
| K030808 |
03/13/2003 |
HANSON MEDICAL CALF IMPLANT |
HANSON MEDICAL, INC. |
| K030809 |
03/13/2003 |
HANSON MEDICAL GLUTEAL IMPLANT |
HANSON MEDICAL, INC. |
| K141822 |
07/07/2014 |
SENSEI X ROBOTIC CATHETER SYSTEM |
HANSON MEDICAL, INC. |
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