Vidacare Corporation is one of 5134 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Vidacare Corporation - FDA 510(k) Cleared Devices
19
Total
19
Cleared
0
Denied
Vidacare Corporation has 19 FDA 510(k) cleared general hospital devices. Based in Irvine, US.
Historical record: 19 cleared submissions from 2004 to 2014.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
Vidacare Corporation — FDA 510(k) Products and Clearance History
19 devices
Cleared
Feb 11, 2014
EZ-IO INTRAOSSEOUS INFUSION SYSTEM
General Hospital
179d
Cleared
Jun 03, 2012
THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE
General Hospital
90d
Cleared
Mar 08, 2012
THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM BY VIDACARE
Gastroenterology & Urology
69d
Cleared
Jul 27, 2010
POWERED PD-IO INFUSION SYSTEM, EZ-IO HUMERAL HEAD, POWERED PH-IO
General Hospital
105d
Cleared
Oct 14, 2009
EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VIDAPORT INTRAOSSEOUS INFUSION...
General Hospital
177d
Cleared
Nov 21, 2008
VERTEBRAL ACCESS SYSTEM BY VIDACARE
General & Plastic Surgery
157d
Cleared
Oct 22, 2007
ONCONTROL BONE MARROW BIOPSY SYSTEM
Gastroenterology & Urology
89d
Cleared
May 21, 2007
POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM
Gastroenterology & Urology
62d
Cleared
Jan 26, 2007
EZ-MIO STERNAL
General Hospital
59d
Cleared
Dec 08, 2006
MANUAL PD-IO
General Hospital
53d
Cleared
Dec 05, 2006
EZ-MIO, EZ-IO DISTAL TIBIA
General Hospital
67d
Cleared
Nov 30, 2006
POWERED EZ-IO BONE MARROW ASPIRATION SYSTEM
Gastroenterology & Urology
70d