Access Scientific, Inc. is one of 19633 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Access Scientific, Inc. - FDA 510(k) Cleared Devices
Recent clearances: THE POWERWAND SAFETY INTRODUCER WITH AND EXTENDED DWELL, THE POWERWAND (R) SAFETY INTRODUCER WITH AN EXTENDED DWELL CATHETER, THE PICC WAND (R) PEELABLE SAFETY INTRODUCER
8
Total
8
Cleared
0
Denied
Access Scientific, Inc. has 8 FDA 510(k) cleared medical devices. Based in San Diego, US.
Historical record: 8 cleared submissions from 2008 to 2012. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Access Scientific, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Access Scientific, Inc.
8 devices
Cleared
Jul 27, 2012
THE POWERWAND SAFETY INTRODUCER WITH AND EXTENDED DWELL
Cardiovascular
43d
Cleared
Jul 15, 2011
THE POWERWAND (R) SAFETY INTRODUCER WITH AN EXTENDED DWELL CATHETER
Cardiovascular
56d
Cleared
Jun 22, 2011
THE PICC WAND (R) PEELABLE SAFETY INTRODUCER
Cardiovascular
61d
Cleared
Mar 22, 2011
THE POWER WAND SAFETY INTRODUCER WITH AN EXTENDED DWELL CATHETER
Cardiovascular
306d
Cleared
Aug 13, 2010
PICC WAND PEELABLE SAFETY INTRODUCER
Cardiovascular
112d
Cleared
Jan 20, 2010
THE PICC WAND PEELABLE SAFETY INTRODUCER
Cardiovascular
113d
Cleared
Mar 30, 2009
THE WAND MICROACCESS SAFETY INTRODUCER
Cardiovascular
45d
Cleared
Dec 04, 2008
THE WAND MICROACCESS SAFETY INTRODUCER, MODELS 90001, 90002, 90005, 90006
Cardiovascular
170d