FDA 510(k) Applications Submitted by EVE CONNER

FDA 510(k) Number Submission Date Device Name Applicant
K000582 02/22/2000 FREESTYLE BLOOD GLUCOSE MONITORING SYSTEM, CAT NO 11001 ABBOTT DIABETES CARE INC.
K970809 03/05/1997 BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL SOMNUS MEDICAL TECHNOLOGIES, INC.
K970837 03/07/1997 SOMNUS MODEL 6000 DISPOSABLE TISSUE COAGULATING ELECTRODE SOMNUS MEDICAL TECHNOLOGIES, INC.
K971450 04/21/1997 SOMNOPLASTY SYSTEM SOMNUS MEDICAL TECHNOLOGIES, INC.
K971711 05/08/1997 SOMNUS MODEL 215 ELECTROSURGICAL GENERATOR SOMNUS MEDICAL TECHNOLOGIES, INC.
K982717 08/04/1998 SOMNOPLASTY SYSTEM, MODELS S2, 1010/2010,2000/1000,1100,3000/30XX/6000, 1200 SOMNUS MEDICAL TECHNOLOGIES, INC.
K973618 09/23/1997 SOMNOPLASTY SYSTEM SOMNUS MEDICAL TECHNOLOGIES, INC.
K973701 09/29/1997 SOMNUS TISSUE COAGULATING ELECTRODE SOMNUS MEDICAL TECHNOLOGIES, INC.
K970838 03/07/1997 SOMNUS MODEL 30XX DISPOSABLE TRI-NEEDLE COAGULATING ELECTRODE SOMNUS MEDICAL TECHNOLOGIES, INC.
K012014 06/12/2001 MODIFICATION TO BLOOD GLUCOSE MONITORING SYSTEM ABBOTT DIABETES CARE INC.
K992684 08/10/1999 FREESTYLE BLOOD GLUCOSE MONITORING SYSTEM ABBOTT DIABETES CARE INC.
K994433 12/30/1999 CONNECT DATA MANAGEMENT SYSTEM ABBOTT DIABETES CARE INC.
K970576 02/13/1997 SOMNUS MODEL 615 ELECTROSURGICAL GENERATOR(MODEL 615) SOMNUS MEDICAL TECHNOLOGIES, INC.


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