510(k) K003299 ยท HLQ Keratoscope, Ac-Powered
OPD-SCAN, MODELS ARK-10000 AND ARK-9000
| Applicant | Nidek Co., Ltd., Lake Forest CA, US |
| Decision | Unknown, Mar 9, 2001 |
| Received | Oct 20, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K003299
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.