510(k) K990257 ยท HKX Tonometer, Ac-Powered
KEELER PULSAIR 3000 NON CONTACT TONOMETER
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Mar 25, 1999 |
| Received | Jan 27, 1999 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K990257
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.