510(k) K821080 ยท HLR Keratoscope, Battery-Powered
HAND KERATOSCOPE
| Applicant | Medical Equipment Designs, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, May 24, 1982 |
| Received | Apr 19, 1982 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K821080
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.