510(k) K073293 ยท HPZ Implant, Eye Sphere
DURETTE IMPLANT
| Applicant | Oculo Plastik, Inc., Montreal, Quebec, CA |
| Decision | Substantially Equivalent, Mar 19, 2008 |
| Received | Nov 23, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K073293
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.