Class Class II

BT-1000 (K232991)

K232991 2024-08-28 Traditional
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Description

BT-1000 by Bistos Co., Ltd. — FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK232991
Clearance Date2024-08-28
Clearance TypeTraditional
Product CodeQGL
Regulation Number882.5898

Categories

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