Class Class II

Accure Laser System (K242035)

K242035 2024-10-11 Traditional
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Description

Accure Laser System by Accure Acne, Inc., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK242035
Clearance Date2024-10-11
Clearance TypeTraditional
Product CodeGEX
Regulation Number878.4810

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