FDA 510(k) Applications for Medical Device Product Code "HLQ"
(Keratoscope, Ac-Powered)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K973756 | EYESYS TECHNOLOGIES, INC. | EYE SYS VISTA | 11/13/1997 |
| K003299 | NIDEK CO., LTD. | OPD-SCAN, MODELS ARK-10000 AND ARK-9000 | 03/09/2001 |
| K964290 | REICHERT OPHTHALMIC INSTRUMENTS, DIV. LEICA, INC. | EYECHEK | 01/09/1997 |
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