Intra Luminal Therapeutics, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intra Luminal Therapeutics, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Intra Luminal Therapeutics, Inc. has 20 FDA 510(k) cleared cardiovascular devices. Based in Carlsbad, US.
Historical record: 20 cleared submissions from 2000 to 2005.
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) Regulatory Record - Intra Luminal Therapeutics, Inc.
20 devices
Cleared
Jun 08, 2005
SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM [PERIPHERAL]
Cardiovascular
57d
Cleared
Jun 07, 2005
SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM [CORONARY]
Cardiovascular
56d
Cleared
Aug 16, 2004
MODIFICATION TO SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Cardiovascular
25d
Cleared
Mar 18, 2004
SAFE-CROSS DEFLECTING CATHETER, MODEL C118ND1
Cardiovascular
22d
Cleared
Mar 03, 2004
MODIFICATION TO SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Cardiovascular
54d
Cleared
Jan 12, 2004
MODIFICATION TO SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Cardiovascular
25d
Cleared
Jan 07, 2004
SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Cardiovascular
190d
Cleared
Dec 11, 2003
MODIFICATION TO SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Cardiovascular
15d
Cleared
Nov 21, 2003
SAFE-CROSS RADIO FREQUENCY TOTAL OCCLUSION CROSSING SYSTEM
Cardiovascular
158d
Cleared
Nov 18, 2003
ILT SAFE-CROSS DEFLECTING CATHETER, MODEL C114ND1
Cardiovascular
71d
Cleared
Aug 22, 2003
SAFE-CROSS DEFLECTING CATHETER, MODEL C114ND1
Cardiovascular
81d
Cleared
Jul 11, 2003
ILT SAFE CROSS 0.035 SUPPORT CATHETER, MODEL C135SN1
Cardiovascular
67d