510(k) K852234 ยท HQF Laser, Ophthalmic
MDS 83 OPHTHALMIC DYE LASER SYSTEM
| Applicant | Meditec, Inc., Clearwater FL, US |
| Decision | Substantially Equivalent, Aug 1, 1985 |
| Received | May 22, 1985 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K852234
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.