FDA 510(k) Applications for Medical Device Product Code "HKM"
(Retinoscope, Battery-Powered)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K964338 | RUDOLF RIESTER GMBH & CO. KG | RI-TINISCOPE-SLIT/RI-TINISCOPE SPOT/RI-VISION-SLIT/RI-VISION-SPOT | 01/09/1997 |
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