510(k) K022280 ยท DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass
STOCKERT CORONARY PERFUSION CANNULAE
| Applicant | Stockert Instrumente GmbH, Morrison CO, US |
| Decision | Substantially Equivalent, Oct 11, 2002 |
| Received | Jul 15, 2002 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K022280
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.