510(k) K885164 ยท HQF Laser, Ophthalmic
LASAG MICRORUPTOR 2 ND:YAG OPHTH. LASER SYSTEM
| Applicant | Chiron Vision Corp., Irvine CA, US |
| Decision | Substantially Equivalent, Jan 10, 1989 |
| Received | Dec 13, 1988 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K885164
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.