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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