Smiths Medical MD, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smiths Medical MD, Inc. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Smiths Medical MD, Inc. has 20 FDA 510(k) cleared general hospital devices. Based in St. Paul, US.
Historical record: 20 cleared submissions from 2004 to 2012.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smiths Medical MD, Inc.
20 devices
Cleared
Feb 09, 2012
SMITH MEDICAL PEEL-AWAY SHEATH INTRODUCERS
Cardiovascular
171d
Cleared
Aug 29, 2011
MEDFUSION MODEL 4000 SYRINGE INFUSION PUMP, PHARMGUARD TOOLBOX 2 MEDICATION...
General Hospital
103d
Cleared
Aug 03, 2010
GRIPPER MICRO BLUNT CANNULA, NON-CORING SAFETY NEEDLE (GRIPPER MICRO NEEDLE)...
General Hospital
98d
Cleared
Jun 12, 2009
LOCKBOX FOR USE WITH MEDFUSION 3000 SERIES PUMPS
General Hospital
50d
Cleared
Dec 17, 2008
CADD -SOLIS MEDICATION SAFETY SOFTWARE: ADMINISTRATOR AND POINT-OF-CARE
General Hospital
85d
Cleared
Jul 18, 2008
CADD MEDICATION CASSETTE RESERVOIR
General Hospital
86d
Cleared
Apr 25, 2008
LOCKBOX FOR USE WITH CADD SOLIS INFUSION PUMP
General Hospital
39d
Cleared
Mar 07, 2008
CADD -SOLIS AMBULATORY INFUSION PUMP AND CADD -SOLIS MEDICATION SAFETY...
General Hospital
218d
Cleared
Feb 13, 2008
CADD-SENTRY PRO MEDICATION SAFETY SOFTWARE-ADMINISTRATOR (21-6275), POINT OF...
General Hospital
117d
Cleared
Dec 14, 2007
POWER PORT-A-CATH, CATH II, AND P.A.S. PORT T2 POWER P.A.C. IMPLANTABLE...
General Hospital
85d
Cleared
Nov 01, 2007
GRIPPER MICRO NEEDLE
General Hospital
98d
Cleared
May 23, 2007
POWER PORT-A-CATH AND POWER PORT-A-CATH II
General Hospital
131d