Caesarea Medical Electronics , Ltd. is one of 503 FDA 510(k) medical device manufacturers from Israel in the dataset, ranked by real submission volume.
Caesarea Medical Electronics , Ltd. - FDA 510(k) Cleared Devices
Recent clearances: T34L SYRINGE DRIVER, BODYGUARD PAIN MANAGER INFUSION SYSTEM, MODIFICATION TO: BODYGUARD INFUSION SYSTEM
9
Total
9
Cleared
0
Denied
Caesarea Medical Electronics , Ltd. has 9 FDA 510(k) cleared medical devices. Based in Caesarea, IL.
Historical record: 9 cleared submissions from 2003 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Caesarea Medical Electronics , Ltd. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Citech as regulatory consultant.
FDA 510(k) Regulatory Record - Caesarea Medical Electronics , Ltd.
9 devices
Cleared
May 16, 2008
T34L SYRINGE DRIVER
General Hospital
43d
Cleared
May 18, 2007
BODYGUARD PAIN MANAGER INFUSION SYSTEM
General Hospital
113d
Cleared
Apr 13, 2007
MODIFICATION TO: BODYGUARD INFUSION SYSTEM
General Hospital
30d
Cleared
Aug 24, 2006
BODYGAURD PAIN MANAGER INFUSION SYSTEM
General Hospital
105d
Cleared
May 12, 2006
MODIFICATION TO BODYGUARD INFUSION PUMP SYSTEM
General Hospital
78d
Cleared
Nov 23, 2005
NIKI T34 AND BODYGUARD T34 SYRINGE DRIVERS
General Hospital
238d
Cleared
Mar 11, 2005
BODYGUARD INFUSION PUMP SYSTEM
General Hospital
162d
Cleared
May 21, 2004
NOA III ENTERAL NUTRITION PUMP
General Hospital
38d
Cleared
Aug 21, 2003
BODYGUARD INFUSION SYSTEM
General Hospital
77d