510(k) K950791 ยท HKM Retinoscope, Battery-Powered
STREAK RETINOSCOPE RX-3
| Applicant | Neitz Instruments Company, Ltd., Tokyo, JP |
| Decision | Substantially Equivalent, Mar 28, 1995 |
| Received | Feb 21, 1995 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K950791
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.