Catheter Innovations, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Catheter Innovations, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
Catheter Innovations, Inc. has 8 FDA 510(k) cleared medical devices. Based in Salt Lake City, US.
Historical record: 8 cleared submissions from 1998 to 2002. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Catheter Innovations, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Catheter Innovations, Inc.
8 devices
Cleared
Jun 06, 2002
VAXCEL PICC WITH PASV VALVE TECHNOLOGY
General Hospital
14d
Cleared
Feb 28, 2001
DUAL LUMEN MIDLINE CATHETER
General Hospital
23d
Cleared
Dec 20, 2000
PLACEMENT-PLUS
General Hospital
23d
Cleared
Dec 03, 1999
CATHETER INNOVATIONS IMPLANTABLE PORT
General Hospital
18d
Cleared
Oct 21, 1999
CATHETER INNOVATIONS IMPLANTABLE PORT
General Hospital
139d
Cleared
May 01, 1998
PASV DUAL LUMEN PERIPHERALLY INSERTED CENTRAL CATHETER (PICC) MODEL NUMBER...
General Hospital
16d
Cleared
May 01, 1998
PASV DUAL LUMEN PERIPHERALLY INSERTED MIDLINE CATHETER MODEL NUMBER...
General Hospital
15d
Cleared
Mar 11, 1998
6 INCH MINI-BONE EXTENSION SET WITH LUER LOCK, NES01S, 6 INCH MIN-BONE...
General Hospital
56d