FDA 510(k) Applications Submitted by FRAN HARRISON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K030438 |
02/11/2003 |
BARD AQUAGUIDE URETERAL CONDUIT |
C.R. BARD, INC. |
| K033778 |
12/04/2003 |
MODIFICATION TO BARD AQUAGUIDE URETERAL CONDUIT |
C.R. BARD, INC. |
| K032521 |
08/15/2003 |
BARD DUAL LUMEN URETERAL CATHETER |
C.R. BARD, INC. |
| K033719 |
11/26/2003 |
BARD TIGERTAIL URETERAL CATHETER |
C.R. BARD, INC. |
| K083733 |
12/16/2008 |
LUME 2 SYSTEM, MODEL GA0005000 |
LUMENIS, LTD. |
| K020713 |
03/05/2002 |
MS-30 LATERAL FEMORAL STEM |
SULZER ORTHOPEDICS, INC. |
| K030792 |
03/12/2003 |
BARD ENDOTRACHEAL TUBE, CUFFED |
C.R. BARD, INC. |
| K001078 |
04/04/2000 |
SULZER ORTHOPEDICS MS-30 FEMORAL STEM |
SULZER ORTHOPEDICS, INC. |
| K031295 |
04/23/2003 |
BARD INNERLACE BIOURETHRAL SUPPORT SYSTEM |
C.R. BARD, INC. |
| K001320 |
04/26/2000 |
SULZER ORTHOPEDICS INC. NATURAL-HIP SYSTEM LD STEM |
SULZER ORTHOPEDICS, INC. |
| K021578 |
05/14/2002 |
NATURAL-KNEE II SYSTEM COCR TIBIAL BASEPLATE |
SULZER ORTHOPEDICS, INC. |
| K992531 |
07/28/1999 |
ULTEGRA SYSTEM ANALYZER, ULTEGRA SYSTEM RPFA-TRAP TEST CARTIDGES, ULTEGRA SYSTEM RPFA-TRAP LEVEL ONE QC, ULTEGRA SYSTEM |
ACCUMETRICS, INC. |
| K002324 |
07/31/2000 |
MODIFIED TO MODULAR FR SEVERE BONE LOSS TRAUMA |
SULZER MEDICA |
| K022985 |
09/09/2002 |
ASCENDENT ACETABULAR SYSTEM |
SULZER ORTHOPEDICS, INC. |
| K013031 |
09/10/2001 |
MOST OPTIONS SYSTEM |
SULZER ORTHOPEDICS, INC. |
| K983295 |
09/21/1998 |
BRAUN THERMOSCAN IRT3020/3500 ONE SECONS EAR THERMOMETER, MODEL IRT3020/3520 |
BRAUN AG |
| K082809 |
09/24/2008 |
ACUPULSE 30 AND 40 CARBON DIOXIDE LASER SYSTEM |
LUMENIS, INC. |
| K964605 |
11/18/1996 |
BRAUN THERMOSCAN PRO-2000 INSTANT THERMOMETER (PRO-2000) |
THERMOSCAN, INC. |
| K043193 |
11/18/2004 |
BARD INLAYOPTIMA URETERAL STENT WITH SUTURE |
C.R. BARD, INC. |
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