Dantec Medical, Inc.
FDA 510(k) & PMA Approved Devices — 25 products
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Total Devices25
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K960503 | DANTEC DUET | FEN | 1996-09-16 | View |
| 510(k) | K950314 | DANTEC MONOPOLAR LUMEN ELECTRODE (13R18 AND 13R19) | GXZ | 1996-03-25 | View |
| 510(k) | K953999 | DANTEC DA CAPO | EXY | 1995-11-21 | View |
| 510(k) | K926363 | MULTI-DOP S | IYO | 1995-06-19 | View |
| 510(k) | K931801 | MULTI-DOP X | IYO | 1995-06-14 | View |
| 510(k) | K930458 | MULTI-DOP L | IYN | 1995-02-03 | View |
| 510(k) | K932059 | NEEDLE ELECTRODES AND DISPOSABLE SCALP ELECTRODE | IKT | 1994-10-04 | View |
| 510(k) | K934580 | DANTEC 13R45 BAR ELECTRODE | GXY | 1994-09-26 | View |
| 510(k) | K931966 | DANTEC DISPOSABLE CONCENTRIC NEEDLE | IKT | 1994-03-30 | View |
| 510(k) | K931923 | DANTEC MAGLITE MAGNETIC STIMULATOR (MAGLITE) | GWF | 1993-11-09 | View |
| 510(k) | K926516 | DANTEC MAGNETIC STIMULATOR MAGPRO | GWF | 1993-08-31 | View |
| 510(k) | K924127 | DANTEC EVOLUTION | GWF | 1993-03-10 | View |
| 510(k) | K923117 | CAVERNOSOMETRY MODULE FOR MENUET | DXT | 1993-02-22 | View |
| 510(k) | K915741 | DISPOSABLE MONOPLAR MEDDLE ELECTRODES | GXE | 1992-12-08 | View |
| 510(k) | K913957 | DANTEC COUNTERPOINT MK2(TM) | GWJ | 1992-01-30 | View |
| 510(k) | K913169 | DANTEC UD 5500 MK2 | FAP | 1992-01-23 | View |
| 510(k) | K914891 | PULLER OPTION FOR ETUDE(TM) | FAP | 1992-01-07 | View |
| 510(k) | K912701 | DANTEC MENUET | FAP | 1991-12-09 | View |
| 510(k) | K911229 | PHOENIX DIGITAL EEG SYSTEM | GWQ | 1991-09-30 | View |
| 510(k) | K913323 | ETUDE (MODEL NUMBERS 24A05 & 24A06) | FAP | 1991-09-23 | View |
No matching devices.
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