Taris Corp.
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) | K880887 | NEOCATH | DWF | 1988-05-24 | View |
| 510(k) | K881256 | NON CORING INFUSION SET | LJT | 1988-04-21 | View |
| 510(k) | K875153 | THIELER KIT | KKX | 1988-02-18 | View |
No matching devices.
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