FDA 510(k) Applications Submitted by DEBORAH L HERRINGTON
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K030627 |
02/27/2003 |
ORBITER PV DIAGNOSTIC ELECTRODE CATHETER, MODELS 320100 & 320110 |
C.R. BARD, INC. |
| K203088 |
10/13/2020 |
Infinity Acute Care System (IACS) Monitoring System |
Draeger Medical Systems, Inc. |
| K050006 |
01/03/2005 |
BOREALIS AMPLIFIER (CLEARSIGN), MODEL 2001232 160 CHANNEL VERSION, 2001267 80 CHANNEL VERSION, 2001268 40 CHANNEL VERSIO |
C.R. BARD, INC. |
| K031000 |
03/31/2003 |
LABSYSTEM III EP LABORATORY W/WINDOWS PLATFORM & WINDOWS EP SOFTWARE VERSION 1.0 |
C.R. BARD, INC. |
| K961271 |
04/02/1996 |
USCI COMMANDER SERIES GUIDE WIRES |
C.R. BARD, INC. |
| K992373 |
07/15/1999 |
ORBITER ST DIAGNOSTIC ELECTRODE CATHETER & ORBITER ST EXTENSION CABLE |
C.R. BARD, INC. |
| K082094 |
07/24/2008 |
BARD PTFE (TEFLON) COATED GUIDE WIRES |
C.R. BARD INC., BARD ELECTROPHYSIOLOGY DIVISION |
| K042105 |
08/04/2004 |
CLIPPER DIAGNOSTIC ELECTRODE CATHETER |
BARD ELECTROPHYSIOLOGY |
| K993000 |
09/07/1999 |
BARD HYDROPHILIC COATED GUIDE WIRES |
C.R. BARD, INC. |
| K983927 |
11/05/1998 |
GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT |
ARTERIAL VASCULAR ENGINEERING, INC. |
| K984627 |
12/30/1998 |
AVE 4F SITESEER CARDIOVASCULAR ANGIOGRAPHIC CATHETER |
ARTERIAL VASCULAR ENGINEERING, INC. |
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