Class Class II

Careverse CoronaryDoc (Careverse CoronaryDoc) (K251656)

K251656 2025-09-04 Traditional
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Description

Careverse CoronaryDoc (Careverse CoronaryDoc) by Careverse Technology Pte. , Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251656
Clearance Date2025-09-04
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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