Endoscopic Technologies, Inc.
FDA 510(k) & PMA Approved Devices — 8 products
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Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K060101 | ESTECH AORTIC EASY FLOW CANNULA | DWF | 2006-05-10 | View |
| 510(k) | K053326 | ESTECH COBRA ELECTROSURGICAL UNIT & CABLE | GEI | 2006-01-06 | View |
| 510(k) | K053100 | ESTECH COBRA BIPOLAR SYSTEM | GEI | 2005-12-19 | View |
| 510(k) | K946105 | ELECTROSURGICAL CUTTING & COAGULATION DEVICE & ACCESSORIES | GEI | 1995-04-06 | View |
| 510(k) | K945978 | TUBING, NONINVASIVE | GAZ | 1995-01-11 | View |
| 510(k) | K945979 | TROCAR/CANNULA | GCJ | 1994-12-21 | View |
| 510(k) | K924057 | DISPOSIBLE ELECTRO COAGULATION PROBE | GEI | 1994-03-11 | View |
| 510(k) | K922685 | TROCARS | GCJ | 1993-04-05 | View |
No matching devices.
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