510(k) K151784 ยท LEL Device, Sleep Assessment
ActTrust
| Applicant | Condor Instruments Ltda. - Epp, Sao Paulo, BR |
| Decision | Substantially Equivalent, May 25, 2016 |
| Received | Jul 1, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151784
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.