510(k) K885017 ยท FLD Apparatus, Hemoperfusion, Sorbent
HEMOSORBA CH-500, CH-350 AND CH-180
| Applicant | Asahi Medical Co., Ltd., Washington DC, US |
| Decision | Substantially Equivalent, Mar 17, 1989 |
| Received | Dec 5, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885017
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.