FDA 510(k) Applications Submitted by Donna Marshall
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K020809 |
03/13/2002 |
MODIFICATION TO CORDIS PALMAZ GENESIS TRANSHEPATIC BILIARY STENT |
CORDIS CORP. |
| K150670 |
03/16/2015 |
STRATAFIX Spiral PDS Plus Knotless Tissue Control Device |
ETHICON, INC. |
| K151200 |
05/05/2015 |
STRATAFIX Spiral MONOCRYL Knotless Tissue Control Device, STRATAFIX Spiral MONOCRYL Plus Knotless Tissue Control Device |
ETHICON, INC. |
| K121442 |
05/15/2012 |
POWERFLEX PRO PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY CATHETER |
CORDIS CORPORATION |
| K181652 |
06/22/2018 |
Coated Vicryl Plus Antibacterial (Polyglactin 910) Absorable Suture |
Ethicon, Inc. |
| K152096 |
07/28/2015 |
DERMABOND Advanced Topical Skin Adhesive, High Viscosity DERMABOND Mini Topical Skin Adhesive |
Ethicon, Inc. |
| K152490 |
09/01/2015 |
DERMABOND PRINEO Skin Closure System |
ETHICON, INC. |
| K042969 |
10/28/2004 |
MODIFICATION TO SMART CONTROL NITINOL STENT TRANSHEPATIC BILIARY SYSTEM |
CORDIS CORP. |
| K023907 |
11/25/2002 |
CORDIS MAXI LD LARGE DIAMETER BALLOON DILATATION CATHETER, CORDIS MAXI LD PTA BALLOON DILATION CATHETER |
CORDIS CORP. |
| K133864 |
12/19/2013 |
DERMABOND PRINEO SKIN CLOSURE SYSTEM |
ETHICON, INC. |
| K034050 |
12/30/2003 |
CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F |
CORDIS CORPORATION |
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