510(k) K013760 ยท HQF Laser, Ophthalmic
DC-3300 LASER DIODE PHOTOCOAGULATOR
| Applicant | Nidek, Inc., Lake Forest CA, US |
| Decision | Substantially Equivalent, Feb 11, 2002 |
| Received | Nov 13, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K013760
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.