510(k) K213875 ยท LFH U.V. Spectrometry, Tricyclic Antidepressant Drugs
DRI TM Tricyclics Serum Tox Assay
| Applicant | Microgenics Corporation, Fremont CA, US |
| Decision | Substantially Equivalent, Dec 21, 2022 |
| Received | Dec 13, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213875
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.