SURGI-VISION GUIDEWIRE COIL— 510(k) K003436
Substantially EquivalentSurgi-Vision, Inc.
FDA 510(k) clearance K003436 for SURGI-VISION GUIDEWIRE COIL, Substantially Equivalent on 2001-02-02. Applicant: Surgi-Vision, Inc..
Clearance details
- Applicant
- Surgi-Vision, Inc.
- Product code
- Code MOS
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Columbia, MD, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.