510(k) K813314 ยท HMX Cannula, Ophthalmic
NLD IMPLANT SET
| Applicant | Design Research Assoc., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 24, 1982 |
| Received | Nov 24, 1981 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K813314
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.