PERCUPASS TUNNELING TOOL MODEL 3452— 510(k) K772013
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K772013 for PERCUPASS TUNNELING TOOL MODEL 3452, Substantially Equivalent on 1977-10-28. Applicant: Medtronic Vascular. Device class: 1.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code HAO
- Device class
- Class 1
- Regulation
- 21 CFR 882.4535
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Walker, MI, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.