510(k) K830008 ยท HLR Keratoscope, Battery-Powered
KARICKHOFF KERATOSCOPE
| Applicant | Surgidev Corp., Mchenry IL, US |
| Decision | Substantially Equivalent, Jan 26, 1983 |
| Received | Jan 3, 1983 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K830008
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.