Class Class II

MR Diffusion Perfusion Mismatch V1.0 (K223502)

K223502 2023-01-13 Traditional
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Description

MR Diffusion Perfusion Mismatch V1.0 by Olea Medical — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK223502
Clearance Date2023-01-13
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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