MODIFICATION TO MODEL 5866-37M LEAD ADAPTOR KIT— 510(k) K000210
Substantially Equivalent - Subject to Tracking Reg.Medtronic Vascular
FDA 510(k) clearance K000210 for MODIFICATION TO MODEL 5866-37M LEAD ADAPTOR KIT, Substantially Equivalent - Subject to Tracking Reg. on 2000-02-23. Applicant: Medtronic Vascular. Device class: 2.
Clearance details
- Applicant
- Medtronic Vascular
- Product code
- Code DTD
- Device class
- Class 2
- Regulation
- 21 CFR 870.3620
- Advisory panel
- Cardiovascular
- Date received
- Decision date
- Decision
- Substantially Equivalent - Subject to Tracking Reg.
- Clearance type
- Special
- Location
- Shoreview, MN, US
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Data sourced from openFDA. This site is unofficial and independent of the FDA.