FDA 510(k) Applications Submitted by CHRIS STUKEL
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K110862 |
03/29/2011 |
VAPRO PLUS INTERMITTENT CATHETER |
HOLLISTER, INCORPORATED |
| K090960 |
04/06/2009 |
VAPRO INTERMITTENT CATHETER, MODEL 72062, 72082,72102, 72122, 72142, 72064, 72084, 72104, 72124,72144, 72164, 72184, |
HOLLISTER, INC. |
| K012372 |
07/26/2001 |
SYSMEX UF-50 |
SYSMEX CORP. |
| K032677 |
08/29/2003 |
SYSMEX POCH-100I |
SYSMEX AMERICA, INC. |
| K083153 |
10/24/2008 |
ACTIFLO INDWELLING BOWEL CATHETER SYSTEM KIT, MODELS: 32004, 32005, 32006, 32007 |
HOLLISTER, INC. |
| K123804 |
12/10/2012 |
INSTAFLO BOWEL CATHETER SYSTEM KIT |
HOLLISTER, INC. |
|
|
