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FDA 510(k) & PMA Approved Devices — 3 products
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Total Devices3
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K080771 | TOP NEUROPOLE NEEDLE, MODEL SH, BL, SC, TC | GXI | 2008-11-10 | View |
| 510(k) | K062946 | TOP NEUROPOLE NEEDLES, MODELS ST, X, RC, XE AND TL | GXI | 2007-02-15 | View |
| 510(k) | K860449 | MODIFICATION TOP ULTRA THINWALL A-V FISTULA NEEDLE | FIE | 1986-02-26 | View |
No matching devices.
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