510(k) K941723 ยท HOO Perimeter, Ac-Powered
WELCH ALLYN GLAUCOMA DETECTOR
| Applicant | Welch Allyn, Inc., Skaneateles Falls NY, US |
| Decision | Substantially Equivalent, Jun 6, 1994 |
| Received | Apr 7, 1994 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K941723
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.