ClearanceBrief
Company ยท US

Pulsion Medical Systems AG

FDA 510(k) clearances and medical device recalls filed under this name, 2000 to 2011. Name variants (Inc, Corp, punctuation) are merged.

8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
DXGComputer, Diagnostic, Pre-Programmed, Single-Function5
KRBProbe, Thermodilution3

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Sep 22, 2011K112448PULSIOFLEX
Pulsion Medical Systems, Inc.
DXG
Jun 18, 2010K091786PULSION PICCO2 (8500), CEVOX OPTICAL MODULE (PC3015), CEVOX DISPOSABLE PROBES (PV2022-30 THRU -38, PV2022-46 THRU -48)
Pulsion Medical Systems AG
DXG
Oct 18, 2007K072735PULSION PICCO-2, MODEL 8500
Pulsion Medical Systems AG
DXG
Sep 19, 2007K072364PULSION PULSIOCATH THERMODILUTION CATHETERS & ACCESSORIES
Pulsion Medical Systems AG
KRB
Jul 25, 2006K060898PULSION PICCO PLUS, MODEL 8100
Pulsion Medical Systems AG
DXG
May 23, 2002K020587PULSION PULSIOCATH PICCO MONITORING KIT, INJECTATE SENSOR TEMPERATURE HOUSING PV 4046
Pulsion Medical Systems AG
KRB
Jun 13, 2000K001762PULSION CONTINUOUS PULSE CONTOUR CARDIAC OUTPUT (PICCO) SYSTEM
Pulsion Medical Systems, Inc.
DXG
May 11, 2000K991886PULSION PULSIOCATH, PULSION PCCO MONITORING KIT, PULSION IN-LINE INJECTATE SENSOR
Pulsion Medical Systems, Inc.
KRB

Latest recalls

DateFirm and productCodeLinked 510(k)
No recalls in this window.
Get alerts for these product codes