Class Class II

OptiLUV Device (K250734)

K250734 2025-09-10 Traditional
Home/ Devices/ OptiLUV Device (K250734)

Description

OptiLUV Device by Pollogen, Ltd., an FDA 510(k) cleared general, plastic surgery device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK250734
Clearance Date2025-09-10
Clearance TypeTraditional
Product CodePBX
Regulation Number878.4400

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