FDA 510(k) Applications Submitted by ANGELA BYLAND

FDA 510(k) Number Submission Date Device Name Applicant
K020344 02/01/2002 RPX TITANIUM CEMNT RESTRICTOR SULZER SPINE-TECH
K060959 04/07/2006 SYMMETRY BALLOON DILATATION CATHETER Boston Scientific Corporation
K091152 04/20/2009 VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM, MODEL 50020 COLOPLAST A/S
K101297 05/10/2010 VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM MODEL 50020 COLOPLAST A/S
K031511 05/14/2003 DYNESYS SPINAL SYSTEM CENTERPULSE SPINE-TECH, INC.
K991707 05/19/1999 MODIFICATION TO ACCESS CEA REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33200, 33205, 33209, 33206 BECKMAN
K011766 06/07/2001 6F EVALUATOR ELECTROPHYSIOLOGY CATHETER, CRD # 402720,402722; 6F EAVUATOR ELECTROPHYSISOLOGY CATHETER, JSN #402721, 4027 ST. JUDE MEDICAL
K022615 08/07/2002 CENTERPULSE, SPINE-TECH DIVISION CEMENT RESTRICTOR CENTERPULSE SPINE-TECH, INC.
K082640 09/10/2008 VIRTUE VENTRAL URETHRAL ELEVATION SLING SYSTEM COLOPLAST MANUFACTURING US, LLC
K003729 12/04/2000 ULTIMUM EV HEMOSTASIS INTRODUCER (14F), ULTIMUM EV HEMOSTASIS INTRODUCER (16F), ULTIMUM EV HEMOSTASIS INTRODUCER (18F), ST. JUDE MEDICAL
K000716 03/03/2000 ACCESS CK-MB ON THE ACCESS IMMUNOASSAY ANALYZER BECKMAN COULTER, INC.
K001935 06/26/2000 ACCESS TESTOSTERONE REAGENTS FOR USE ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 33560, 33565 BECKMAN COULTER, INC.


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