510(k) K964751 ยท HQF Laser, Ophthalmic
CERALAS DIODE LASER SYSTEM (CERALAS D2)
| Applicant | Ceram Optec, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Feb 21, 1997 |
| Received | Nov 26, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964751
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.