FDA 510(k) Applications Submitted by SURGI-VISION, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K111073 |
04/18/2011 |
SURGIVISION INC. CLEARPOINT SYSTEM |
SURGI-VISION, INC. |
| K992193 |
06/29/1999 |
ENDO-ESOPHAGEAL MR COIL |
SURGI-VISION, INC. |
| K003436 |
11/06/2000 |
SURGI-VISION GUIDEWIRE COIL |
SURGI-VISION, INC. |
| K020495 |
02/14/2002 |
INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL |
SURGI-VISION, INC. |
| K020790 |
03/11/2002 |
INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND INTERCEPT VASCULAR INTERNAL MR COIL |
SURGI-VISION, INC. |
| K011781 |
06/07/2001 |
INTERCEPT-URETHRAL MICROCOIL |
SURGI-VISION, INC. |
| K002345 |
08/02/2000 |
SURGI-VISION URETHRAL COIL |
SURGI-VISION, INC. |
| K002916 |
09/19/2000 |
SURGI-VISION PROSTATE COIL |
SURGI-VISION, INC. |
| K994436 |
12/30/1999 |
SURGI-VISION ESOPHAGEAL STYLET COIL |
SURGI-VISION, INC. |
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