Class Class I

K5 (K233805)

K233805 2024-09-03 Traditional
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Description

K5 by Osstem Implant Co., Ltd. Chair Business — FDA 510(k) cleared dental device.

Regulatory Information

Device ClassClass Class I
510(k) NumberK233805
Clearance Date2024-09-03
Clearance TypeTraditional
Product CodeEIA
Regulation Number872.6640

Categories

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