510(k) K810810 ยท DHX System, Test, Carcinoembryonic Antigen
AMICON ULTRAFILTRATION MEMBRANES CMII
| Applicant | Amicon, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Apr 17, 1981 |
| Received | Mar 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K810810
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.