Retinalabs.Com
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K003036 | TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025 | KYG | 2000-12-22 | View |
| 510(k) | K000418 | PDT DOSECALCULATOR, MODEL 80000 | NDC | 2000-10-24 | View |
| 510(k) | K000457 | VERTEFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 11000 SERIES; PHOTOFUSION-PHOTODYNAMIC THERAPY PAK, MODEL 12000 SERIES | HMX | 2000-05-09 | View |
| 510(k) | K000420 | SILICONE OIL EXPRESS (INFUSION PAK), MODELS 10000, 10001, 10002, 10003 | MRH | 2000-05-08 | View |
| 510(k) | K000416 | TRANSPAK (VITREORETINAL INFUSION PAK), MODELS 90000, 90001 | MPA | 2000-05-08 | View |
No matching devices.
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