Class Class II

Edwards MC3 Tricuspid annuloplasty ring (4900) (K251982)

K251982 2025-09-23 Abbreviated
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Description

Edwards MC3 Tricuspid annuloplasty ring (4900) by Edwards Lifesciences, LLC, an FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251982
Clearance Date2025-09-23
Clearance TypeAbbreviated
Product CodeKRH
Regulation Number870.3800

Categories

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