510(k) K911721 ยท HKX Tonometer, Ac-Powered
KEELER PULSAIR NON CONTACT TONOMETER, MODIFICATION
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Jun 25, 1991 |
| Received | Apr 17, 1991 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K911721
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.