Nitinol Medical Technologies, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nitinol Medical Technologies, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Nitinol Medical Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Los Angles, US.
Historical record: 7 cleared submissions from 1990 to 1997. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Nitinol Medical Technologies, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Nitinol Medical Technologies, Inc.
7 devices
Cleared
Apr 16, 1997
SIMON NITINOL FILTER/STRAIGHT LINE SYSTEM
Cardiovascular
93d
Cleared
Nov 18, 1996
SIMON NITINOL FILTER/STRAIGHT LINE SYSTEM
Cardiovascular
108d
Cleared
Nov 18, 1996
SIMON NITINOL FILTER SYSTEM
Cardiovascular
108d
Cleared
Apr 28, 1995
SIMON NITINOL FILTER
Cardiovascular
241d
Cleared
Aug 09, 1994
SIMON NITINOL FILTER
Cardiovascular
196d
Cleared
Oct 17, 1991
SIMON NITINOL FILTER, MODIFICATION
Cardiovascular
157d
Cleared
Apr 20, 1990
SIMON NITINOL FILTER
Cardiovascular
270d