INTERCEPT-URETHRAL MICROCOIL— 510(k) K011781
Substantially EquivalentSurgi-Vision, Inc.
FDA 510(k) clearance K011781 for INTERCEPT-URETHRAL MICROCOIL, Substantially Equivalent on 2001-08-31. Applicant: Surgi-Vision, Inc.. Device class: 2.
Clearance details
- Applicant
- Surgi-Vision, Inc.
- Product code
- Code MOS
- Device class
- Class 2
- Regulation
- 21 CFR 892.1000
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Gaithersburg, MD, US
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More clearances from Surgi-Vision, Inc.
view all- 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
- K003436 — SURGI-VISION GUIDEWIRE COIL
- K002916 — SURGI-VISION PROSTATE COIL
Data sourced from openFDA. This site is unofficial and independent of the FDA.