510(k) K942180 ยท HQF Laser, Ophthalmic
KEELER MULTILASE 3000
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Nov 22, 1994 |
| Received | May 4, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K942180
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.