510(k) K964338 ยท HKM Retinoscope, Battery-Powered
RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT
| Applicant | Rudolf Riester GmbH & Co. KG, D-72417 Jungingen, DE |
| Decision | Substantially Equivalent, Jan 9, 1997 |
| Received | Oct 31, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K964338
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.