Class Class II

Clearview Intracoronary Shunts (K253998)

K253998 2026-01-20 Special
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Description

Clearview Intracoronary Shunts by Medtronic, Inc., an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK253998
Clearance Date2026-01-20
Clearance TypeSpecial
Product CodeDWF
Regulation Number870.4210

Categories

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