Class Class II

HESTIA (L200-A) (K242946)

K242946 2025-10-03 Traditional
Home/ Devices/ HESTIA (L200-A) (K242946)

Description

HESTIA (L200-A) by Senbitec Co., Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242946
Clearance Date2025-10-03
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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