510(k) K231469 · PJE Blood/Plasma Collection Device For Dna Testing
PAXgene® Blood DNA Tube
| Applicant | Preanalytix GmbH, Hombrechtikon, CH |
| Decision | Substantially Equivalent, Jun 21, 2023 |
| Received | May 22, 2023 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K231469
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.