FDA 510(k) Applications Submitted by APRIL LAVENDER
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K950118 |
01/11/1995 |
ABRM CATHETER |
COOK, INC. |
K980390 |
02/02/1998 |
PTA BALLOON CATHETER |
COOK, INC. |
K990726 |
03/05/1999 |
ENVY GUIDING CATHETER |
COOK, INC. |
K990753 |
03/08/1999 |
GRAC HIGH DOSE RATE (HDR) REMOTE AFTERLOADING CATHETER |
COOK, INC. |
K961668 |
04/30/1996 |
MICROFERRET CATHETER |
COOK, INC. |
K021557 |
05/13/2002 |
SPECTRUM SILICONE CATHETER |
COOK, INC. |
K981886 |
05/29/1998 |
VRAC HIGH DOSE RATE (HDR) REMOTE AFTERLOADING CATHETER |
COOK, INC. |
K981906 |
06/01/1998 |
MODIFICATION FOR PTA BALLOON CATHETER |
COOK, INC. |
K962167 |
06/05/1996 |
BRONCHIAL BLOCKER |
COOK, INC. |
K011812 |
06/11/2001 |
SPECTRUM VENTRICULAR CATHETER |
COOK, INC. |
K021920 |
06/11/2002 |
7.0 FR. ENDOBRONCHIAL BLOCKER |
COOK, INC. |
K991985 |
06/14/1999 |
COOK HIGH VOLUME INFUSION ADAPTER INTRAVASCULAR ADMINISTRATION SET |
COOK, INC. |
K001985 |
06/29/2000 |
INTRODEUCE DOUBLE LUMEN INTRODUCER |
COOK, INC. |
K982333 |
07/02/1998 |
MODIFICATION TO ULDALL DOUBLE LUMEN HEMODIALYSIS CATHETER SET AND TRAY |
COOK, INC. |
K962761 |
07/16/1996 |
REIGEL TUNNELING DEVICE |
COOK, INC. |
K982500 |
07/20/1998 |
CHAIT CECOSTOMY CATHETER |
COOK, INC. |
K002254 |
07/25/2000 |
COOK PRESSURE MONITORING CATHETER |
COOK, INC. |
K002288 |
07/27/2000 |
ARNDT PEDIATRIC ENDOBRONCHIAL BLOCKER |
COOK, INC. |
K972800 |
07/28/1997 |
PTA BALLOON CATHETER |
COOK, INC. |
K963565 |
09/05/1996 |
MRI NEEDLES |
COOK, INC. |
K983217 |
09/14/1998 |
ROWE DUAL-CHECK VALVE |
COOK, INC. |
K973565 |
09/19/1997 |
QUICK-CARE BIOPSY NEEDLE |
COOK, INC. |
K983771 |
10/26/1998 |
STRATEGY CORONARY WIRE GUIDE |
COOK, INC. |
K974774 |
12/22/1997 |
ENVY GUIDING CATHETER |
COOK, INC. |
K962097 |
05/29/1996 |
VENTRICULAR CATHETER SET |
COOK, INC. |
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