Class Class II

PRAEVAorta®2 (K243859)

K243859 2025-08-29 Traditional
Home/ Devices/ PRAEVAorta®2 (K243859)

Description

PRAEVAorta®2 by Nurea, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK243859
Clearance Date2025-08-29
Clearance TypeTraditional
Product CodeQIH
Regulation Number892.2050

Categories

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