FDA 510(k) Applications Submitted by DENNIS S MADISON

FDA 510(k) Number Submission Date Device Name Applicant
K000824 03/14/2000 PERCUTANEOUS INTRODUCER, MODEL 10383-XXX MEDAMICUS, INC.
K953734 07/17/1995 LUMAX(MODIFICATION) MEDAMICUS, INC.
K990705 03/04/1999 MEDAMICUS COAXIAL INTRODUCER KIT, 10330-XXX, BOSTON SCIENTIFIC COAXIAL DILATOR SET MEDAMICUS, INC.
K011085 04/10/2001 GUIDEWIRE INTRODUCER SAFETY NEEDLE MEDAMICUS, INC.
K971911 04/28/1997 LUMAX CYSTOMETRY ADMINISTRATION TUBE SET MEDAMICUS, INC.
K013120 09/18/2001 PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18 MEDAMICUS, INC.


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