510(k) K032213 ยท DWA Control, Pump Speed, Cardiopulmonary Bypass
STOCKERT CENTRIFUGAL PUMP SYSTEM WITH TUBING CLAMP
| Applicant | Stockert Instrumente GmbH, North Attleboro MA, US |
| Decision | Substantially Equivalent, Aug 29, 2003 |
| Received | Jul 21, 2003 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K032213
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.