510(k) K080739 ยท MKZ Dna Probe, Nucleic Acid Amplification, Chlamydia
ABBOTT REALTIME CT/NG ASSAY AND MULTI-COLLECT SPECIMEN COLLECTION KIT
| Applicant | Abbott Molecular, Inc., Des Plaines IL, US |
| Decision | Substantially Equivalent, Jul 10, 2008 |
| Received | Mar 17, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K080739
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.