Class Class II

AccuContour 4.0 (K251351)

K251351 2026-01-23 Traditional
Home/ Devices/ AccuContour 4.0 (K251351)

Description

AccuContour 4.0 by Manteia Technologies Co., Ltd., an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK251351
Clearance Date2026-01-23
Clearance TypeTraditional
Product CodeQKB
Regulation Number892.2050

Categories

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