510(k) K123514 ยท NXC Aligner, Sequential
CLEARPATH ALIGNER
| Applicant | Qserve America, Inc., Charlestown NH, US |
| Decision | Substantially Equivalent, Nov 1, 2013 |
| Received | Nov 14, 2012 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K123514
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.