Surgi-Vision, Inc.
FDA 510(k) & PMA Approved Devices — 9 products
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Total Devices9
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K111073 | SURGIVISION INC. CLEARPOINT SYSTEM | ORR | 2011-06-22 | View |
| 510(k) | K020790 | INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND INTERCEPT VASCULAR INTERNAL MR COIL | MOS | 2002-05-21 | View |
| 510(k) | K020495 | INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL | MOS | 2002-04-23 | View |
| 510(k) | K011781 | INTERCEPT-URETHRAL MICROCOIL | MOS | 2001-08-31 | View |
| 510(k) | K003436 | SURGI-VISION GUIDEWIRE COIL | MOS | 2001-02-02 | View |
| 510(k) | K002916 | SURGI-VISION PROSTATE COIL | MOS | 2000-11-28 | View |
| 510(k) | K002345 | SURGI-VISION URETHRAL COIL | MOS | 2000-10-11 | View |
| 510(k) | K994436 | SURGI-VISION ESOPHAGEAL STYLET COIL | MOS | 2000-03-14 | View |
| 510(k) | K992193 | ENDO-ESOPHAGEAL MR COIL | MOS | 1999-09-03 | View |
No matching devices.
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