Stockert Instrumente GmbH
Stockert Instrumente GmbH appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on September 23, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K042374 | STOCKERT SCP RHYTHM | September 23, 2004 |
| K041558 | STOCKERTIR PURGE CONTROL (APC) SYSTEM | July 2, 2004 |
| K032213 | STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP | August 29, 2003 |
| K023622 | STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35 | November 21, 2002 |
| K022280 | STOCKERT CORONARY PERFUSION CANNULAE | October 11, 2002 |
| K022321 | STOCKERT V172-28 VENOUS FEMORAL CANNULA | October 9, 2002 |
| K020571 | STOCKERT CENTRIFUGAL PUMP CONSOLE | September 23, 2002 |
| K011838 | CENTRIFUGAL PUMP | February 5, 2002 |
| K011088 | SIII ALARM AMPLIFIER | May 2, 2001 |