510(k) K992635 ยท KRI Accessory Equipment, Cardiopulmonary Bypass
INTERFACE MODULE IDDD
| Applicant | Stoeckert Instrumente, North Attleboro MA, US |
| Decision | Substantially Equivalent, Dec 20, 1999 |
| Received | Aug 6, 1999 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K992635
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.