510(k) K900080 ยท HPZ Implant, Eye Sphere
NEW IOWA MOTILITY IMPLANT
| Applicant | Oculo Plastik, Inc., Montreal, Quebec Canada, CA |
| Decision | Substantially Equivalent, Mar 23, 1990 |
| Received | Jan 4, 1990 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K900080
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.