Novoste Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Novoste Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Novoste Corp. has 5 FDA 510(k) cleared medical devices. Based in Miami, US.
Historical record: 5 cleared submissions from 1988 to 1995. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Novoste Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Novoste Corp.
5 devices
Cleared
Dec 28, 1995
NOVOSTE PULSE PLUS BLOOD CONTAINMENT DEVICE
Cardiovascular
556d
Cleared
Apr 24, 1991
NOVOSTE GUIDING CATHETER
Cardiovascular
20d
Cleared
Jul 17, 1990
MODIFIED NOVOSTE ANGIOGRAPHIC CATHETER
Cardiovascular
168d
Cleared
Jan 24, 1990
MODIFIED ANGIOGRAPHIC CATHETER
Cardiovascular
57d
Cleared
Aug 09, 1988
NOVOSTE 4, 4.2, 5 AND 6 FRENCH CATHETERS
Cardiovascular
238d