510(k) K901887 ยท CAK Microfilter, Blood Transfusion
MODIFIED SEPACELL R-SERIES BLOOD FILTERS
| Applicant | Asahi Medical Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Aug 8, 1990 |
| Received | Apr 26, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K901887
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.