Surgi-Vision, Inc.
Surgi-Vision, Inc. holds FDA 510(k) medical device clearances, first cleared 1999, most recent 2011.
Top product codes for Surgi-Vision, Inc.
Recent clearances by Surgi-Vision, Inc.
- K111073 — SURGIVISION INC. CLEARPOINT SYSTEM
- K020790 — INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL MICROCOIL, AND INTERCEPT VASCULAR INTERNAL MR COIL
- K020495 — INTERCEPT ESOPHAGEAL INTERNAL MR COIL, INTERCEPT URETHRAL INTERNAL MR COIL, AND INTERCEPT VASCULAR INTERNAL MR COIL
- K011781 — INTERCEPT-URETHRAL MICROCOIL
- K003436 — SURGI-VISION GUIDEWIRE COIL
- K002916 — SURGI-VISION PROSTATE COIL
- K002345 — SURGI-VISION URETHRAL COIL
- K994436 — SURGI-VISION ESOPHAGEAL STYLET COIL
- K992193 — ENDO-ESOPHAGEAL MR COIL
Data sourced from openFDA. This site is unofficial and independent of the FDA.