FDA 510(k) Applications Submitted by NEIL BURRIS
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080432 |
02/19/2008 |
MAPERSOL |
PRESERVATION SOLUTIONS, INC. |
| K111139 |
04/22/2011 |
DERMA PRENE ISOTOUCH GREEN STERILE POWDER-FREE POLYISOPRENE SURGICAL GOVES, TESTED FOR U |
ANSELL HEALTHCARE PRODUCTS, INC. |
| K091245 |
04/28/2009 |
COSTORSOL |
PRESERVATION SOLUTIONS, INC. |
| K102189 |
08/02/2010 |
POWDER FREE NITRLE EXAMINATION GLOVES WITH CHEMOTHERAPY LABELING CLAIM |
LATEXX MANUFACTURING SDN.BHD. |
| K052296 |
08/23/2005 |
CLIRPATH TURBO EXCIMER LASER CATHETERS |
SPECTRANETICS CORP. |
| K052514 |
09/14/2005 |
CLIRPATH TURBO PLUS EXCIMER LASER CATHETERS, MODELS 314-151, 314-159, 317-152, 317-156, 320-006, 320-159, 323-001 |
SPECTRANETICS CORP. |
| K103043 |
10/14/2010 |
COLORADO CATHETER STERILESURE - NEW NAME PERFIC CATH |
ADAPTA MEDICAL, INC |
| K083453 |
11/21/2008 |
COSTORSOL |
PRESERVATION SOLUTIONS, INC. |
| K073693 |
12/31/2007 |
COSTORSOL |
PRESERVATION SOLUTIONS, INC. |
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