510(k) K930437 ยท HLF Device, Measuring, Lens Radius, Ophthalmic
MARCO STANDARD RADIUSGAUGES
| Applicant | Marco Ophthalmic, Inc., Jacksonville FL, US |
| Decision | Substantially Equivalent, Aug 9, 1993 |
| Received | Jan 26, 1993 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K930437
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.