Sontek Corp.
3 FDA 510(k) clearances · Manufacturer
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| Record | Firm | Date |
|---|---|---|
| PERIPHERAL TRANSLUMINAL ARGIOPLASTY (K832279) | Sontek Corp. | 1983-11-14 |
| SONTEK INFUSION CATHETER (K831562) | Sontek Corp. | 1983-06-30 |
| SONTEK ANGIOGRAPHIC CATHETER (K810508) | Sontek Corp. | 1981-04-17 |
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