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FDA 510(k) Applications for Medical Device Product Code "HMX"
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| FDA 510(k) Number | Applicant | Device Name | Decision Date |
| K970873 | AMERICAN MEDICAL DEVICES, INC. | ENDOSOFT SOFT TIP NEEDLE (20 GA. AND 19 GA.) | 05/20/1997 |
| K010305 | MICRON SURGICAL, INC. | WEISS RETINAL CANNULA | 05/02/2001 |
| K000457 | RETINALABS.COM | VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES | 05/09/2000 |