Datascope Corp., Patient Monitoring Division is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Datascope Corp., Patient Monitoring Division - FDA 510(k) Cleared Dev...
4
Total
4
Cleared
0
Denied
Datascope Corp., Patient Monitoring Division has 4 FDA 510(k) cleared medical devices. Based in Mahwah, US.
Historical record: 4 cleared submissions from 2008 to 2013. Primary specialty: Anesthesiology.
Browse the FDA 510(k) cleared devices submitted by Datascope Corp., Patient Monitoring Division Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Datascope Corp., Patient Monitoring Division
4 devices
Cleared
Feb 14, 2013
A5 ANESTHESIA DELIVERY SYSTEM
Anesthesiology
125d
Cleared
Jul 15, 2009
PASSPORT V MONITOR, MODEL 0998-00-6100
Cardiovascular
23d
Cleared
May 08, 2009
ACCUTORR V MONITOR, MODEL 0998-00-2000
Cardiovascular
24d
Cleared
Jun 09, 2008
NAVIGATOR ANESTHESIA DELIVERY SYSTEM, MODEL 0998-00-3024-01
Anesthesiology
137d