510(k) K893171 ยท HKL Retinoscope, Ac-Powered
VISTA STREAK RETINOSCOPE (AC-POWERED)
| Applicant | Keeler Instruments, Inc., Broomall PA, US |
| Decision | Substantially Equivalent, Sep 21, 1989 |
| Received | Apr 25, 1989 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K893171
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.