Class Class II

HiRise (1040-230) (K241713)

K241713 2024-07-12 Special
Home/ Devices/ HiRise (1040-230) (K241713)

Description

HiRise (1040-230) by Curvebeam, LLC — FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241713
Clearance Date2024-07-12
Clearance TypeSpecial
Product CodeJAK
Regulation Number892.1750

Categories

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