510(k) K891610 ยท HOD Clamp, Eyelid, Ophthalmic
HENSON CFA 3000 CENTRAL VISUAL FIELD SCREENER
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Jun 5, 1989 |
| Received | Mar 20, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K891610
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.