510(k) K954842 ยท KYG Device, Irrigation, Ocular Surgery
D.O.R.C. VFI/VFE SYSTEM
| Applicant | Dutch Ophthalmic USA, Inc., Kingston NH, US |
| Decision | Substantially Equivalent, Apr 15, 1996 |
| Received | Oct 23, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K954842
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.