510(k) K231329 ยท LSL Dna-Reagents, Neisseria
Aptima Neisseria gonorrhoeae Assay
| Applicant | Hologic, Inc., San Diego CA, US |
| Decision | Substantially Equivalent, Jan 26, 2024 |
| Received | May 8, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231329
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.