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FDA 510(k) Applications for Medical Device Product Code "HKO"
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FDA 510(k) Number | Applicant | Device Name | Decision Date |
K031831 | TOPCON MEDICAL SYSTEMS, INC. | TOPCON MODEL BV-1000 AUTOMATED SUBJECTIVE REFRACTION SYSTEM | 12/19/2003 |
K000327 | VISX, INCORPORATED | WAVESCAN WAVEFRONT SYSTEM MODEL HS 1 | 05/02/2000 |