510(k) K823767 ยท HLF Device, Measuring, Lens Radius, Ophthalmic
ERG-JET ELECTRODE
| Applicant | Life-Tech Intl., Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 8, 1983 |
| Received | Dec 14, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K823767
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.