Class Class II

VEGA (K242859)

K242859 2025-09-19 Traditional
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Description

VEGA by Ibramed Equipamentos Médicos, an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242859
Clearance Date2025-09-19
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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