FDA 510(k) Applications Submitted by MEDAMICUS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K954093 |
08/09/1995 |
LUMAX (MODIFICATION) |
MEDAMICUS, INC. |
| K965167 |
12/24/1996 |
PERCUTANEOUS VENOUS INTRODUCER 10264 |
MEDAMICUS, INC. |
| K000824 |
03/14/2000 |
PERCUTANEOUS INTRODUCER, MODEL 10383-XXX |
MEDAMICUS, INC. |
| K953734 |
07/17/1995 |
LUMAX(MODIFICATION) |
MEDAMICUS, INC. |
| K994097 |
12/03/1999 |
MEDAMICUS EPIDURAL INTRODUCER |
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. |
| K040150 |
01/23/2004 |
MODIFICATION TO MEDAMICUS FLOWGUARD PEELABLE INTRODUCER |
MEDAMICUS, INC. |
| K030905 |
03/24/2003 |
MEDAMICUS FLOWGUARD PEELABLE INTRODUCER |
MEDAMICUS, INC. |
| K021004 |
03/28/2002 |
VALVED PEELABLE INTRODUCER |
MEDAMICUS, INC. |
| K022689 |
08/13/2002 |
MODIFICATION TO MEDAMICUS AXIA RSN |
MEDAMICUS, INC. |
| K020563 |
02/20/2002 |
MEDAMICUS AXIA RSN |
MEDAMICUS, INC. |
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