510(k) K223921 ยท DHX System, Test, Carcinoembryonic Antigen
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| Applicant | Beckman Coulter, Inc., Chaska MN, US |
| Decision | Substantially Equivalent, Sep 22, 2023 |
| Received | Dec 29, 2022 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K223921
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.