510(k) K990900 ยท HNO Keratome, Ac-Powered
MICROKERATOME, MODEL MK-2000
| Applicant | Nidek, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Sep 24, 1999 |
| Received | Mar 18, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990900
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.