510(k) K951079 ยท HQF Laser, Ophthalmic
NIDEK MODEL GYC-1500 AND GYC-2000
| Applicant | Nidek, Inc., Fremont CA, US |
| Decision | Substantially Equivalent, Sep 14, 1995 |
| Received | Mar 9, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K951079
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.