FDA 510(k) Applications for Medical Device Product Code "HLX"
(Photostimulator, Ac-Powered)
| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K983983 | ELECTRO-DIAGNOSTIC IMAGING, INC. | EDI VERIS SYSTEM | 02/03/1999 |
| K003442 | ELECTRO-DIAGNOSTIC IMAGING, INC. | MODIFICATION TO EDI VERIS SYSTEM | 05/04/2001 |
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