Company ยท US
Stockert Instrumente GmbH
FDA 510(k) clearances and medical device recalls filed under this name, 2001 to 2004. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 23, 2004 | K042374 | STOCKERT SCP RHYTHM Stockert Instrumente GmbH | DWA |
| Jul 2, 2004 | K041558 | STOCKERTIR PURGE CONTROL (APC) SYSTEM Stockert Instrumente GmbH | DTW |
| Aug 29, 2003 | K032213 | STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP Stockert Instrumente GmbH | DWA |
| Nov 21, 2002 | K023622 | STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35 Stockert Instrumente GmbH | DWF |
| Oct 11, 2002 | K022280 | STOCKERT CORONARY PERFUSION CANNULAE Stockert Instrumente GmbH | DWF |
| Oct 9, 2002 | K022321 | STOCKERT V172-28 VENOUS FEMORAL CANNULA Stockert Instrumente GmbH | DWF |
| Sep 23, 2002 | K020571 | STOCKERT CENTRIFUGAL PUMP CONSOLE Stockert Instrumente GmbH | DTQ |
| Feb 5, 2002 | K011838 | CENTRIFUGAL PUMP Stockert Instrumente GmbH | DWA |
| May 2, 2001 | K011088 | SIII ALARM AMPLIFIER Stockert Instrumente GmbH | DTQ |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||