Pulsion Medical Systems, Inc. is one of 19863 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pulsion Medical Systems, Inc. - FDA 510(k) Cleared Devices
Recent clearances: PULSIOFLEX, PULSION CONTINUOUS PULSE CONTOUR CARDIAC OUTPUT (PICCO) SYSTEM, PULSION PULSIOCATH, PULSION PCCO MONITORING KIT, PULSION IN-LINE INJECTATE SENSOR
3
Total
3
Cleared
0
Denied
Pulsion Medical Systems, Inc. has 3 FDA 510(k) cleared medical devices. Based in Cornelius, US.
Historical record: 3 cleared submissions from 2000 to 2011. Primary specialty: Cardiovascular.
Browse the FDA 510(k) cleared devices submitted by Pulsion Medical Systems, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pulsion Medical Systems, Inc.
3 devices