Intensive Technology, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Intensive Technology, Inc. - FDA 510(k) Cleared Devices
12
Total
12
Cleared
0
Denied
Intensive Technology, Inc. has 12 FDA 510(k) cleared cardiovascular devices. Based in Mchenry, US.
Historical record: 12 cleared submissions from 1981 to 1993.
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 - Intensive Technology, Inc.
12 devices
Cleared
Jan 13, 1993
INTRA-OPERATIVE TEC ATHERECTOMY SYSTEM
Cardiovascular
208d
Cleared
Aug 24, 1992
TEC ROTATING DUAL HEMOVALVE
Cardiovascular
433d
Cleared
Oct 16, 1991
IVT GUIDING CATHETER
Cardiovascular
173d
Cleared
Jan 03, 1991
IVT INTRODUCER SHEATH
Cardiovascular
155d
Cleared
Nov 29, 1990
HEMOCHRON(R) HEPARIN RESPONSE TEST
Hematology
92d
Cleared
Jun 28, 1990
MODIFIED IVT PERIPHERAL ATHERECTOMY
Cardiovascular
72d
Cleared
Mar 06, 1990
MODIFIED IVT PERIPHERAL ATHERECTOMY SYSTEM
Cardiovascular
119d
Cleared
Jan 04, 1990
IVT 0.014 GUIDE WIRE
Cardiovascular
90d
Cleared
Jun 22, 1989
APTT BY HEMOCHRON(R)
Hematology
80d
Cleared
May 23, 1989
PERIPHERAL ATHERECTOMY SYSTEM
Cardiovascular
111d
Cleared
Oct 28, 1988
0.014 PERIPHERAL GUIDE WIRE
Cardiovascular
113d
Cleared
Jan 26, 1981
RESPA-TROL
Chemistry
10d