Promex, Inc.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K023450 | BIOPSY SITE TISSUE MARKER DEVICE | NEU | 2002-12-19 | View |
| 510(k) | K022634 | CO-AXIAL INTRODUCER NEEDLE | DYB | 2002-11-06 | View |
| 510(k) | K010400 | VACUUM ASSISTED CORE BIOPSY DEVICE | KNW | 2001-07-24 | View |
| 510(k) | K011270 | AUTOMATED CORE BIOPSY DEVICE | FCG | 2001-06-22 | View |
| 510(k) | K001132 | BONE BIOPSY NEEDLE | KNW | 2000-05-01 | View |
| 510(k) | K994272 | AUTOMATED CORE BIOPSY DEVICE | KNW | 2000-01-07 | View |
| 510(k) | K993435 | MANUAL BONE MARROW BIOPSY DEVICE | KNW | 1999-12-06 | View |
| 510(k) | K973184 | PROSTATE SEEDING NEEDLE | IWJ | 1997-11-21 | View |
| 510(k) | K972865 | PROMEX ENT TISSUE REMOVAL SYSTEM | ERL | 1997-09-29 | View |
| 510(k) | K961078 | AUTOMATED VITRECTOMY DEVICE | HQE | 1996-06-14 | View |
| 510(k) | K960023 | KIRSHNER WIRES (K-WIRE) & STEINMANN PINS | JDW | 1996-03-18 | View |
| 510(k) | K960405 | SPINAL NEEDLE | MIA | 1996-02-28 | View |
| 510(k) | K955168 | SURGICAL CUTTER | GEI | 1996-01-22 | View |
| 510(k) | K954265 | TROCAR STYLE NEEDLE/CO-AXIAL INTRODUCER NEEDLE | KNW | 1995-09-29 | View |
| 510(k) | K954231 | AUGASTROENTEROLOGY-UROLOGY BIOPSY INSTRUMENT | FCG | 1995-09-22 | View |
| 510(k) | K954155 | GREENE, TURNER, MENGHINI STYLE ASPIRATION BIOPSY NEEDLE | FCG | 1995-09-12 | View |
| 510(k) | K945146 | CHIBA, FRANSEEN, WESTCOTT, SPINAL STYLE ASPIRATION BIOPSY NEEDLE | FCG | 1994-12-21 | View |
| 510(k) | K945124 | BREAST LESION LOCALIZATION NEEDLE | GDF | 1994-11-22 | View |
No matching devices.
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