Surgi-Vision, Inc.
Surgi-Vision, Inc. appears in FDA public data with 0 recalls, 9 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on June 22, 2011.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 0
- Compliance Actions
- 0
Known Names
surgivision, surgi-vision
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K111073 | SURGIVISION INC. CLEARPOINT SYSTEM | June 22, 2011 |
| K020790 | INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND INTERCEPT VASCULAR INTERNAL | May 21, 2002 |
| K020495 | INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR I | April 23, 2002 |
| K011781 | INTERCEPT-URETHRAL MICROCOIL | August 31, 2001 |
| K003436 | SURGI-VISION GUIDEWIRE COIL | February 2, 2001 |
| K002916 | SURGI-VISION PROSTATE COIL | November 28, 2000 |
| K002345 | SURGI-VISION URETHRAL COIL | October 11, 2000 |
| K994436 | SURGI-VISION ESOPHAGEAL STYLET COIL | March 14, 2000 |
| K992193 | ENDO-ESOPHAGEAL MR COIL | September 3, 1999 |