Class Class II

CEREGLIDE 71 Intermediate Catheter (K221930)

K221930 2023-03-09 Traditional
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Description

CEREGLIDE 71 Intermediate Catheter by Cerenovus, Inc. — FDA 510(k) cleared cardiovascular device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK221930
Clearance Date2023-03-09
Clearance TypeTraditional
Product CodeQJP
Regulation Number870.1250

Categories

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