FDA 510(k) Applications Submitted by Glen Norton
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K141408 |
05/28/2014 |
RESOLVE BILIARY LOCKING DRAINAGE CATHETER |
MERIT MEDICAL SYSTEMS, INC. |
| K030020 |
01/03/2003 |
HEMOSPLIT LONG-TERM HEMODIALYSIS CATHETER |
C.R. BARD, INC. |
| K050049 |
01/10/2005 |
DYNAFLO BYPASS GRAFT |
BARD PERIPHERAL VASCULAR, INC. |
| K030268 |
01/27/2003 |
NIAGARA TEMPORARY DUAL LUMEN CATHETERS; FLEXXICON II TEMPORARY DUAL LUMEN CATHETERS |
C.R. BARD, INC. |
| K030277 |
01/27/2003 |
SOFT-CELL DUAL LUMEN CATHETERS |
C.R. BARD, INC. |
| K042036 |
07/29/2004 |
AIRGUARD VALVED INTRODUCER |
C.R. BARD, INC. |
| K092343 |
08/04/2009 |
EN SNARE ENDOVASCULAR SNARE SYSTEM |
MERIT MEDICAL SYSTEMS, INC. |
| K052282 |
08/22/2005 |
VENAFLO II VASCULAR GRAFT |
BARD PERIPHERAL VASCULAR, INC. |
| K062832 |
09/21/2006 |
VACORA 14G BIOPSY PROBES, MODELS VB14116, VB14138 |
C.R. BARD, INC. |
| K033294 |
10/14/2003 |
HEMOSPLIT XK, HEMOSPLIT XK CATHETER, 16FR X 42 CM, KIT;16FR X 19 CM, KIT WITH MICROINTRODUCER |
C.R. BARD, INC. |
|
|
