Class Class II

SurgiTwin (K250290)

K250290 2025-08-29 Traditional
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Description

SurgiTwin by Twinsight, an FDA 510(k) cleared radiology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250290
Clearance Date2025-08-29
Clearance TypeTraditional
Product CodeLLZ
Regulation Number892.2050

Categories

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