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FDA 510(k) Applications Submitted by SUSAN D SCOTT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K090084
01/12/2009
ELATION ENDOVENOUS LASER PROCEDURE KIT UNIVERSAL FLUID DISPENSING SYRINGE
MERIT MEDICAL SYSTEMS, INC.
K060812
03/24/2006
POWERPORT(TM)IMPLANTED TITANIUM PORT W/8 FR. CHRONOFLEX CATHETER-MULTIPLE
C.R. BARD, INC.
K063118
10/11/2006
BARD BALLOON DILATION KIT WITH TRIFUNNEL GASTROSTOMY TUBE
C.R. BARD, INC.
K072215
08/09/2007
TITANIUM POWERPORT ISP IMPLANTED PORT
C.R. BARD, INC.
K072549
09/10/2007
TITANIUM POWERPORT ISP IMPLANTED PORT WITH 6 FR CHRONOFLEX POLYURETHANE CATHETER
C.R. BARD, INC.
K083523
11/26/2008
MONARCH COMPAK INFLATION SYRINGE AND UNIVERSAL FLUID DISPENSING SYRINGE
MERIT MEDICAL SYSTEMS, INC.
K073423
12/05/2007
MRI POWERPORT IMPLANTED PORT WITH 9.6 FR SILICONE CATHETER
C.R. BARD, INC.
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