MODIFICATION TO EXPORT ASPIRATION CATHETER— 510(k) K030201
Substantially EquivalentMedtronic Vascular
FDA 510(k) clearance K030201 for MODIFICATION TO EXPORT ASPIRATION CATHETER, Substantially Equivalent on 2003-03-26. Applicant: Medtronic Vascular. Device class: 2.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code NFA
- Device class
- Class 2
- Regulation
- 21 CFR 870.1250
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Location
- Danvers, MA, US
Recent devices under product code NFA
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Data sourced from openFDA. This site is unofficial and independent of the FDA.