FDA 510(k) Applications Submitted by Kathleen Roberts
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060573 |
03/06/2006 |
BURBANK TENACULUM |
VASCULAR CONTROL SYSTEMS, INC |
| K031358 |
04/30/2003 |
TRANSVAGINAL DOPPLER PROBE |
VASCULAR CONTROL SYSTEMS, INC |
| K032125 |
07/10/2003 |
CSTAT, MODELS 09-0014-01 AND 09-0014-02 |
VASCULAR CONTROL SYSTEMS, INC |
| K982797 |
08/10/1998 |
BLUNT T-PEEL INTRODUCER MODEL NUMBER PE-16PICB, PE-18PICB, PE-20PICB, PE-24PICB |
LUTHER MEDICAL PRODUCTS, INC. |
| K052209 |
08/15/2005 |
VCS DOPPLER TRANSCEIVER, MODEL 09-0023-01 |
VASCULAR CONTROL SYSTEMS, INC |
| K102496 |
08/31/2010 |
POWERHEART AED G3 SEMI-AUTOMATIC, POWERHEART AED G3 AUTOMATIC, POWERHEART AED G3 PRO, POWERHEART AED G3 PLUS |
CARDIAC SCIENCE CORPORATION |
| K122758 |
09/10/2012 |
POWERHEART G5 AED |
CARDIAC SCIENCE CORPORATION |
| K143714 |
12/29/2014 |
Powerheart G5 AED |
CARDIAC SCIENCE CORPORATION |
|
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