DeviceClearance

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.

Clearance details

Applicant
Medtronic Vascular
Product code
Code DTD
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.