510(k) K864037 ยท HJB Instrument, Measuring, Corneal Radius
KERASCAN MODEL 2000 KERATOGRAPHIC AUTO ANALYZER
| Applicant | Kera Corp., Santa Clara CA, US |
| Decision | Substantially Equivalent, Nov 13, 1986 |
| Received | Oct 16, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K864037
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.