FDA 510(k) Applications Submitted by ROBERT CHIN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060721 |
03/17/2006 |
LARIAT LOOP APPLICATOR |
SENTREHEART |
| K041590 |
06/14/2004 |
AUTODETECT SYRINGE |
INDIGO ORB, INC. |
| K022008 |
06/19/2002 |
CARDIMA ABLATION SYSTEM |
CARDIMA, INC. |
| K030049 |
01/06/2003 |
MODIFICATION TO RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086 |
RUBICOR MEDICAL, INC. |
| K020047 |
01/07/2002 |
RUBICOR BREAST BIOPSY DEVICE |
RUBICOR MEDICAL, INC. |
| K100649 |
03/08/2010 |
SOUNDBITE HEARING SYSTEM BY SONITUS |
SONITUS MEDICAL INC |
| K070803 |
03/23/2007 |
INVIVODENTAL |
ANATOMAGE, INC |
| K961245 |
04/01/1996 |
HEARTPORT ENDOPULMONARY VENT |
HEARTPORT, INC. |
| K961270 |
04/02/1996 |
HEARTPORT ENDOSINUS CATHETER |
HEARTPORT, INC. |
| K071048 |
04/13/2007 |
RUBICOR MAGIC BREAST BIOPSY DEVICE, MODEL 31537 |
RUBICOR MEDICAL, INC. |
| DEN130004 |
05/06/2013 |
MOERAE SURGICAL MARKING PEN |
MOERAE MATRIX, INC. |
| K061387 |
05/18/2006 |
VERESURE BELL |
VERESURE, INC. |
| K131659 |
06/06/2013 |
MOERAE VEIN PREPARATION KIT |
MOERAE MATRIX, INC. |
| K962510 |
06/27/1996 |
HEARTPORT ENDOAORTIC CLAMP |
HEARTPORT, INC. |
| K962835 |
07/22/1996 |
HEARTPORT ENDOVENOUS DRAINAGE CANNULA |
HEARTPORT, INC. |
| K962858 |
07/22/1996 |
HEARTPORT ENDOVASCULAR CARDIOPULMONARY BYPASS SYSTEM ANTEGRADE SYTEM (CATALOG NUMBER ECPB-A) ANTEGRADE/RETROGRADE SYSTEM |
HEARTPORT, INC. |
| K032584 |
08/21/2003 |
RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30629 |
RUBICOR MEDICAL, INC. |
| K082543 |
09/03/2008 |
SONOCINE ADJUNCTIVE BREAST ULTRASOUND SYSTEM (ABU), MODEL 100 |
SONOCINE, INC. |
| K052506 |
09/13/2005 |
RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 31108 |
RUBICOR MEDICAL, INC. |
| K023601 |
10/28/2002 |
RUBICOR ENCAPSULE BREAST BIOPSY DEVICE, MODEL 30086 |
RUBICOR MEDICAL, INC. |
| K053151 |
11/10/2005 |
RUBICOR MAGIC BREAST BIOPSY DEVICE |
RUBICOR MEDICAL, INC. |
| K110831 |
03/25/2011 |
SOUNDBITE HEARING SYSTEM BY SONITUS MEDICAL |
SONITUS MEDICAL INC |
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