Epimed International, Inc.
FDA 510(k) & PMA Approved Devices — 13 products
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Total Devices13
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K200624 | Percutaneous Introducer | BSO | 2020-04-27 | View |
| 510(k) | K190256 | Rulo Radiofrequency Lesion Probe | GXI | 2019-03-08 | View |
| 510(k) | K053318 | RX EPIDURAL NEEDLE | BSP | 2006-02-17 | View |
| 510(k) | K051171 | STINGRAY EPIDURAL CATHETER CONNECTOR | CAZ | 2005-08-26 | View |
| 510(k) | K051860 | FLEXIBLE INTRODUCER CANNULA, MODEL 135-1837 | MIA | 2005-08-22 | View |
| 510(k) | K043467 | FLEXIBLE SPINAL NEEDLE | BSP | 2005-03-31 | View |
| 510(k) | K041021 | RF INTRODUCTION CANNULA | GXI | 2004-09-16 | View |
| 510(k) | K041843 | PENCIL POINT NEEDLE | BSP | 2004-08-24 | View |
| 510(k) | K023140 | VERSA-KATH EPIDURAL CATHETER, MODEL 156-2124 | BSO | 2003-08-15 | View |
| 510(k) | K030562 | TUOHY EPIDURAL NEEDLE | BSP | 2003-04-03 | View |
| 510(k) | K022029 | QUINCKE SPINAL NEEDLE | BSP | 2002-07-30 | View |
| 510(k) | K020926 | EXTENSION SET, MODELS 1911-512 | FPA | 2002-07-12 | View |
| 510(k) | K981329 | FETH-R-KATH | BSO | 1998-08-26 | View |
No matching devices.
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