510(k) K073506 ยท NSU Instrumentation For Clinical Multiplex Test Systems
LUMINEX LX 100/200 INSTRUMENT
| Applicant | Luminex Corp., Toronto, CA |
| Decision | Substantially Equivalent, Mar 7, 2008 |
| Received | Dec 13, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073506
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.