Class Class II

SUPER VELOCE (K241699)

K241699 2024-08-13 Traditional
Home/ Devices/ SUPER VELOCE (K241699)

Description

SUPER VELOCE by Ilooda Co,., Ltd. — FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK241699
Clearance Date2024-08-13
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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