Class Class II

System Sophi (K250501)

K250501 2025-11-14 Traditional
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Description

System Sophi by This AG, an FDA 510(k) cleared ophthalmic device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250501
Clearance Date2025-11-14
Clearance TypeTraditional
Product CodeHQC
Regulation Number886.4670

Categories

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