510(k) K864639 ยท HLR Keratoscope, Battery-Powered
REUSABLE SURGICAL KERATOSCOPE
| Applicant | Jedmed Instrument Co., St. Louis MO, US |
| Decision | Substantially Equivalent, Dec 29, 1986 |
| Received | Nov 26, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864639
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.