Pulsion Medical Systems AG
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K112448 | PULSIOFLEX | September 22, 2011 |
| K091786 | PULSION PICCO2 (8500), CEVOX OPTICAL MODULE (PC3015), CEVOX DISPOSABLE PROBES (PV2022-30 THRU -38, | June 18, 2010 |
| K072735 | PULSION PICCO-2, MODEL 8500 | October 18, 2007 |
| K072364 | PULSION PULSIOCATH THERMODILUTION CATHETERS & ACCESSORIES | September 19, 2007 |
| K060898 | PULSION PICCO PLUS, MODEL 8100 | July 25, 2006 |
| K020587 | PULSION PULSIOCATH PICCO MONITORING KIT, INJECTATE SENSOR TEMPERATURE HOUSING PV 4046 | May 23, 2002 |
| K001762 | PULSION CONTINUOUS PULSE CONTOUR CARDIAC OUTPUT (PICCO) SYSTEM | June 13, 2000 |
| K991886 | PULSION PULSIOCATH, PULSION PCCO MONITORING KIT, PULSION IN-LINE INJECTATE SENSOR | May 11, 2000 |