510(k) K102740 ยท NQX System, Nucleic Acid Amplification Test, Dna, Methicillin Resistant Staphylococcus Aureus, Direct Specimen
NUCLISENS EASYQ MRSA; NUCLISENS EASYQ ANALYZER; NUCLISENS EASYQ INCUBATOR (110 VOLT); NUCLISENS DIRECTOR V.2.6
| Applicant | bioMerieux, Inc., Durham NC, US |
| Decision | Substantially Equivalent, May 20, 2011 |
| Received | Sep 22, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102740
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.