510(k) K981567 ยท LSL Dna-Reagents, Neisseria
HYBRID CAPTURE II CT/GC TEST
| Applicant | Digene Corp., Beltsville MD, US |
| Decision | Substantially Equivalent, Feb 29, 2000 |
| Received | May 1, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K981567
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.