Acist Medical Systems is one of 5135 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Acist Medical Systems - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Acist Medical Systems has 7 FDA 510(k) cleared medical devices. Based in Eden Prairie, US.
Historical record: 7 cleared submissions from 1999 to 2014. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Acist Medical Systems Filter by specialty or product code using the sidebar.
Acist Medical Systems — FDA 510(k) Products and Clearance History
7 devices
Cleared
Jan 30, 2014
CARDIOVASCULAR PRESSURE MEASUREMENT (CPM) SYSTEM, NAVVUS CATHETER
Cardiovascular
176d
Cleared
Jan 27, 2003
ACIST GENTOO CONTRAST INJECTION SYSTEM
Cardiovascular
314d
Cleared
Apr 26, 2002
ACIST PLUS 4 ANGIOGRAPHIC CATHETER
Cardiovascular
28d
Cleared
May 31, 2000
MODIFICATION TO ACIST CL 100H
Cardiovascular
426d
Cleared
Mar 28, 2000
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R-2000
Cardiovascular
85d
Cleared
Dec 07, 1999
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL CL1OOH
Cardiovascular
29d
Cleared
Feb 11, 1999
ACIST INJECTOR SYSTEM, MODEL CL100 H
Cardiovascular
90d