Class Class II

DLP™ Silicone Coronary Artery Ostial Cannulae (K230960)

K230960 2023-05-04 Special
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Description

DLP™ Silicone Coronary Artery Ostial Cannulae by Medtronic, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK230960
Clearance Date2023-05-04
Clearance TypeSpecial
Product CodeDWF
Regulation Number870.4210

Categories

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