510(k) K885154 ยท KRJ Filter, Prebypass, Cardiopulmonary Bypass
INTERSEPT* CRYSTALLOID CARDIOPLEGIA DELIV. SYSTEM
| Applicant | Medtronic Blood Systems, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Feb 22, 1989 |
| Received | Dec 15, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885154
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.