510(k) K860011 ยท HQB Photocoagulator And Accessories
NIDEK AC-2000 LASER SYSTEM
| Applicant | Nidek, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Feb 7, 1986 |
| Received | Jan 3, 1986 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K860011
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.