Stockert Instrumente GmbH
North Attleboro, MA, US
Stockert Instrumente GmbH appears in FDA device records in North Attleboro, MA. FDA records list 9 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 9
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 9 510(k) clearances for Stockert Instrumente GmbH between 2001 and 2004. The busiest year on record is 2002, with 5. The most recent is 2004, with 2.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 2001 | 1 |
| 2002 | 5 |
| 2003 | 1 |
| 2004 | 2 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K042374 | STOCKERT SCP RHYTHM | DWA | Substantially Equivalent | |
| K041558 | STOCKERTIR PURGE CONTROL (APC) SYSTEM | DTW | Substantially Equivalent | |
| K032213 | STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP | DWA | Substantially Equivalent | |
| K023622 | STOCKERT PEDIATRIC AORTIC CANNULAE, MODEL NUMBERS A272-15 THROUGH A272-35 | DWF | Substantially Equivalent | |
| K022280 | STOCKERT CORONARY PERFUSION CANNULAE | DWF | Substantially Equivalent | |
| K022321 | STOCKERT V172-28 VENOUS FEMORAL CANNULA | DWF | Substantially Equivalent | |
| K020571 | STOCKERT CENTRIFUGAL PUMP CONSOLE | DTQ | Substantially Equivalent | |
| K011838 | CENTRIFUGAL PUMP | DWA | Substantially Equivalent | |
| K011088 | SIII ALARM AMPLIFIER | DTQ | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain