Company ยท US
Surgi-Vision, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2011. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 22, 2011 | K111073 | SURGIVISION INC. CLEARPOINT SYSTEM Surgi-Vision, Inc. | ORR |
| May 21, 2002 | K020790 | INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND INTERCEPT VASCULAR INTERNAL MR COIL Surgi-Vision, Inc. | MOS |
| Apr 23, 2002 | K020495 | INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL Surgi-Vision, Inc. | MOS |
| Aug 31, 2001 | K011781 | INTERCEPT-URETHRAL MICROCOIL Surgi-Vision, Inc. | MOS |
| Feb 2, 2001 | K003436 | SURGI-VISION GUIDEWIRE COIL Surgi-Vision, Inc. | MOS |
| Nov 28, 2000 | K002916 | SURGI-VISION PROSTATE COIL Surgi-Vision, Inc. | MOS |
| Oct 11, 2000 | K002345 | SURGI-VISION URETHRAL COIL Surgi-Vision, Inc. | MOS |
| Mar 14, 2000 | K994436 | SURGI-VISION ESOPHAGEAL STYLET COIL Surgi-Vision, Inc. | MOS |
| Sep 3, 1999 | K992193 | ENDO-ESOPHAGEAL MR COIL Surgi-Vision, Inc. | MOS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||