510(k) K103532 ยท LRG Instrument For Auto Reader & Interpretation Of Overnight Suscept. Systems
AUTOREADER 2
| Applicant | Trek Diagnostic Systems, Cleveland OH, US |
| Decision | Substantially Equivalent, Aug 26, 2011 |
| Received | Dec 1, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103532
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.