510(k) K882136 ยท KRD Device, Vascular, For Promoting Embolization
INTERSEPT* OXYGEN GAS LINE FILTER
| Applicant | Medtronic Blood Systems, Inc., Anaheim CA, US |
| Decision | Substantially Equivalent, Aug 11, 1988 |
| Received | May 20, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K882136
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.