510(k) K161673 ยท LZU Plug, Punctum
LacriPro Punctum Plug
| Applicant | Lacrimedics, Inc., Dupont WA, US |
| Decision | Substantially Equivalent, Nov 18, 2016 |
| Received | Jun 16, 2016 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K161673
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.