510(k) K872846 ยท HQF Laser, Ophthalmic
NIDEK ADC-8000 LASER SYSTEM
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Oct 15, 1987 |
| Received | Jul 20, 1987 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K872846
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.