Thomas Medical Products, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thomas Medical Products, Inc. - FDA 510(k) Cleared Devices
23
Total
23
Cleared
0
Denied
Thomas Medical Products, Inc. has 23 FDA 510(k) cleared cardiovascular devices. Based in Malvern, US.
Historical record: 23 cleared submissions from 1990 to 2013.
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 - Thomas Medical Products, Inc.
23 devices
Cleared
Jan 29, 2013
HEARTSPAN STEERABLE INTRODUCER KIT
Cardiovascular
172d
Cleared
Aug 14, 2012
CORONARY SINUS GUIDE AND LATERAL VEIN INTRODUCER KITS
Cardiovascular
209d
Cleared
Sep 23, 2010
GUIDE CATHETERS AND ACCESSORIES
Cardiovascular
164d
Cleared
Feb 03, 2009
CROSSOVER
Cardiovascular
90d
Cleared
May 14, 2008
REINFORCED CATHETER INTRODUCER SYSTEM (RCIS)
Cardiovascular
1d
Cleared
Jan 04, 2008
Y-GLIDE
Cardiovascular
99d
Cleared
Feb 15, 2005
LARGE BORE SPLITTABLE INTRODUCER KIT
Cardiovascular
63d
Cleared
Jun 01, 2004
MODIFICATION TO BRAIDED GUIDING INTRODUCER SYSTEM
Cardiovascular
75d
Cleared
May 02, 2002
TRANSSEPTAL NEEDLE/TROCAR
Cardiovascular
332d
Cleared
Feb 11, 2002
MODIFICATION TO TRANSSEPTAL INTRODUCER SET
Cardiovascular
32d
Cleared
Oct 23, 2001
MODIFICATION TO BRAIDED GUIDING INTRODUCER
Cardiovascular
28d
Cleared
Jul 19, 2001
SPLITTABLE SHEATH INTRODUCER KIT
Cardiovascular
204d