Medamicus, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Medamicus, Inc. has 20 FDA 510(k) cleared cardiovascular devices. Based in Minneapolis, US.
Historical record: 20 cleared submissions from 1989 to 2004.
Browse the complete list of FDA 510(k) cleared cardiovascular devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) cleared devices by Medamicus, Inc.
20 devices
Cleared
Feb 18, 2004
MODIFICATION TO MEDAMICUS FLOWGUARD PEELABLE INTRODUCER
Cardiovascular
26d
Cleared
Apr 09, 2003
MEDAMICUS FLOWGUARD PEELABLE INTRODUCER
Cardiovascular
16d
Cleared
Aug 23, 2002
MODIFICATION TO MEDAMICUS AXIA RSN
Cardiovascular
10d
Cleared
Jun 06, 2002
VALVED PEELABLE INTRODUCER
Cardiovascular
70d
Cleared
May 21, 2002
MEDAMICUS AXIA RSN
Cardiovascular
90d
Cleared
Jan 24, 2002
PERCUTANEOUS INTRODUCER SET, MODEL 042294 AND KIT MODEL 3550-18
Neurology
128d
Cleared
Jul 09, 2001
GUIDEWIRE INTRODUCER SAFETY NEEDLE
Cardiovascular
90d
Cleared
Apr 13, 2000
PERCUTANEOUS INTRODUCER, MODEL 10383-XXX
Cardiovascular
30d
Cleared
Mar 01, 2000
MEDAMICUS EPIDURAL INTRODUCER
Neurology
89d
Cleared
Jun 28, 1999
MEDAMICUS COAXIAL INTRODUCER KIT, 10330-XXX, BOSTON SCIENTIFIC COAXIAL...
Cardiovascular
116d
Cleared
Jul 25, 1997
PERCUTANEOUS VENOUS INTRODUCER 10264
Cardiovascular
213d
Cleared
Jun 03, 1997
LUMAX CYSTOMETRY ADMINISTRATION TUBE SET
Gastroenterology & Urology
36d